Phosphonomonoester nucleic acids process for their preparation and their use

ABSTRACT

Novel oligonucleotide analogs of the formula [I] are described, ##STR1## in which A, B, D, G, L, P, Q, Q&#39;, R 5 , R 6 , X, Y, Z and n are as defined in the description, which have useful physical, biological and pharmacological properties, as well as a process for their preparation. Their application relates to use as inhibitors of gene expression (antisense oligonucleotides, ribozymes, sense oligonucleotides and triplex-forming oligonucleotides), as probes for the detection of nucleic acids and as auxiliaries in molecular biology.

This is a continuation of application Ser. No. 08/613,417, filed Mar. 11, 1996, now U.S. Pat. No. 5,874,553, which is incorporated herein by reference.

The present invention relates to novel oligonucleotide analogs having useful physical, biological and pharmacological properties, and to a process for their preparation. Their application relates to use as inhibitors or gene expression (antisense oligonucleotides, ribozymes, sense oligonucleotides and triplex-forming oligonucleotides), as probes for the detection of nucleic acids and as auxiliaries in molecular biology.

The disclosure of all documents referred to in this specification are incorporated in whole by reference.

Oligonucleotides are applied to a growing extend as inhibitors of gene expression (J. F. Milligan, M. D. Matteucci and J. C. Martin, J. Med. Chem. 36 (1993) 1923; E. Uhlmann and A. Peyman, Chemical Reviews 90 (1990) 543; S. T. Crooke, Annu. Rev. Pharmacol. Toxicol. 32 (1992) 329).

Antisense oligonucleotides are nucleic acid fragments whose base sequence is complementary to an mRNA to be inhibited. This target mRNA can be of cellular, viral or other pathogenic origin. Possible cellular target sequences are, for example, those of receptors, enzymes, growth factors, immunomodulators, ion channels or oncogenes. The inhibition of virus replication with the aid of antisense oligonucleotides was described, for example, for RSV (rous sarcoma virus), HSV-1 and -2 (herpes simplex virus type I and II), HIV (human immunodeficiency virus) and influenza viruses. In this case, oligonucleotides are employed which are complementary to the viral nucleic acid.

The sequence of sense oligonucleotides is designed, however, such that they bind ("capture"), for example, nucleic acid-binding proteins or nucleic acid-processing enzymes and thus inhibit their biological activity (C. Helene and J. J. Toulme, Biochim. Biophys. Acta 1049 (1990) 99). Viral targets which may be mentioned here are, for example, reverse transcriptase, DNA polymerase and transactivator proteins. In general, triplex-forming oligonucleotides have DNA as a target and, after binding to this, form a triple helical structure.

Whereas with the aid of the antisense oligonucleotides, the processing (splicing etc.) of the mRNA or its translation into the protein are in general inhibited, triplex-forming oligonucleotides inhibit the transcription or replication of the DNA (N. T. Thuong, and C. Helene, Angew. Chem. 105 (1993) 697; Uhlmann and Peyman, Chemical Reviews 90 (1990) 543). However, it is also possible to bind single-stranded nucleic acids with an antisense oligonucleotide in a first hybridization with formation of a double strand, which then forms a triplex structure in a second hybridization with a triplex-forming oligonucleotide. The antisense and triplex-binding regions can in this case either be accommodated in two separate oligonucleotides or else in one oligonucleotide.

A further application of synthetic oligonucleotides are the so-called ribozymes, which destroy the target RNA as a result of their ribonuclease activity (D. Castanotto, J. J. Rossi, J. O. Deshler, Critical Rev. Eukar. Gene Expr. 2 (1992) 331).

In DNA diagnosis, nucleic acid fragments with suitable labelling are employed as so-called DNA probes for the specific hybridization of a nucleic acid to be detected. The specific formation of the new double strand is in this case monitored with the aid of the labelling, which is preferably not radioactive. In this manner, genetic, malignant, viral or other pathogen-caused diseases can be detected.

For most applications mentioned, oligonucleotides in their naturally occurring form are not very suitable or completely unsuitable. They must be chemically modified such that they meet the specific requirements. In order that oligonucleotides can be employed in biological systems, for example for the inhibition of virus replication, they must fulfill the following requirements:

1. They must have a sufficiently high stability under in vivo conditions, i.e. both in serum and intracellularly.

2. They must be constituted such that they can pass through the cell and nucleus membrane.

3. They must bind to their target nucleic acid in base-specific manner under physiological conditions in order to display the inhibitory effect.

These requirements are not indispensable for DNA probes; however, these oligonucleotides must be derivatized such that detection is possible, for example by means of fluorescence, chemiluminescence, colorimetry or specific staining (Beck and Koster, Anal. Chem. 62 (1990) 2258).

A multiplicity of chemical variations of oligonucleotides are known which have been synthesized with the aim of fulfilling the abovementioned requirements better than the unmodified oligonucleotides. The chemical modification of the oligonucleotides is usually carried out by appropriately modifying the phosphate backbone, ribose unit or the nucleobases (Uhlmann and Peyman, Chemical Review 90 (1990) 543). The modifications also include those in which both the phosphate bridge and the sugar unit have been replaced by other groups, for example by "morpholinonucleoside" oligomers (E. P. Stirchak et al., Nucleic Acids Res. 17 (1989) 6129) or "PNAs" (P. E. Nielsen et al, Bioconj. Chem. 5 (1994) 3). PNAs, in particular, are distinguished by unusually high affinities for target RNA, but suffer from other unfavorable properties such as lack of solubility or deficient cell penetration (W. Wang et al., Tetrahedron Letters 36 (1995) 1181; M. Egholm et al., in "Innovation and Perspectives in Solid Phase Synthesis, Peptides, Proteins, Nucleic Acids", Roger Epton, Ed. Mayflower Worldwide Limited, Birmingham, 1994, 145-148).

It is therefore an object to find novel oligonucleotide analogs having favorable properties.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is a graph showing a UV-Absorbance Profile Versus Temperature for [pmena-t9] in the Presence of 1 eq. dA9 [See Example 56].

FIG. 2 is a chart showing proof of PMENA-DNA binding by Gel-Shift [See Example 57].

The invention therefore relates to compounds of the formula I ##STR2## wherein n is a number from zero to 100;

B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkylthio, an aromatic group or a heterocyclic group, where alkyl, aryl, the aromatic or a heterocyclic group, where alkyl, aryl, the aromatic or heterocyclic group can optionally be substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, --C(O)OH, oxo, --C(O)R⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₆)-alkoxyalkyl, --S(O)_(m) R⁸, -(C₁ -C₆)-alkyl- S(O)_(m) R₈, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, --NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NR⁹ R¹⁰ or --NR⁹ C(═O)NR⁹ R¹⁰,

m is zero, 1 or 2

B independently or one another is a natural nucleobase, an unnatural nucleobase or a reporter ligand; and

A-B can also be a D- or L-amino acid condensed on via the carboxyl group or peptides consisting of these amino acids having a length of up to 5 amino acid residues,

L independently of one another is N or R¹ N⁺, and

R¹ is hydrogen or (C₁ -C₆)-alkyl which can be substituted by hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio or amino. Preferably, R¹ is hydrogen or methyl;

A independently of one another is a single bond, a methylene group or a group of the formula IIa or IIb; ##STR3##

Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above;

M is a single bond, --O--, --S-- or --NR¹ --, where R¹ is as defined above;

R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, such as F, Cl or Br, or (C₁ -C₆)-alkyl which can optionally be substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio, but are preferably hydrogen;

p and q independently of one another are zero to 5;

r and s independently of one another are zero to 5;

D and G each represent CR⁵ R⁶ which can be the same or different;

R⁵ and R⁶ independently of another are hydrogen, (C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, and alkyl and aryl can optionally be substituted by SR¹ or NR¹ R^(1'), where R^(1') is as defined above and R^(1') independently or R¹ has the same meaning as R¹, but R⁵ and R⁶ are preferably hydrogen;

X is --O--, --S-- or --NR¹ --, in which R¹ is as defined above;

Y is ═O or ═S;

Z is --OR⁸, --NR⁹ R¹⁰ or X'Q", where X' is defined as X and Q" is defined as Q;

R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₁ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl can be substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and aryl can be substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰, but preferably R⁸ is hydrogen, (C₁ -C₄)-alkyl, (C₆ -C₁₂)-aryl or (C₆ C₁₂)-aryl-(C₁ -C₆)-alkyl, where aryl can be monosubstituted by (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br or NO₂. More preferably R⁸ is hydrogen, (C₁ -C₆)-alkyl, phenyl or 2-(4-nitrophenyl)ethyl;

R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₁ -C₁₈)-alkenyl, (C₁ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl can be substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl, or Br, or R⁹ and R¹⁰ can together form a 4 to 7-membered ring together with the N atom carrying them;

Q and Q' independently of one another are hydrogen or R⁸.

Alternatively, Q and Q' are conjugates which a) favorably affect the properties of antisense oligonucleotides, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a label of a DNA probe, d) during the hybridization of the oligonucleotide analog to the target nucleic acid, attack the target nucleic acid through binding or crosslinking. Or, Q and Q' are oligonucleotides which can be unmodified or modified, where the following variants are intended to be examples of some modifications (e.g. described in E. Uhlmann and A. Peyman, Chemical Reviews 90 (1990) 543; "Protocols for Oligonucleotides and Analogs", Synthesis and Properties & Synthesis and Analytical Techniques, S. Agrawal, Ed. Humana Press, Totowa, USA (1993):

a) complete or partial replacement of the 3'-and/or the 5'-phosphoric acid diester bridges, for example by phosphorothioate, phosphorodithioate, NR⁴ R^(4') -phosphoramidate, boranophosphate, phosphate-(C₁ -C₂₁)-O-alkyl ester, phosphate-[(C₆ -C₁₂)aryl-(C₁ -C₂₁)-O-alkyl] ester, 2,2,2-trichlorodimethylethylphosphonate, (C₁ -C₈)alkylphosphonate or (C₆ -C₁₂)-arylphosphonate bridges, where R⁴ and R^(4') independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₁₄)-aryl-(C₁ -C₈)-alkyl or --(CH₂)_(c) -[NH(CH₂)_(c) ]_(d) -NR⁷ R⁷, in which c is an integer from 2 to 6 and d is an integer from 0 to 6, and R⁷ independently of one another is hydrogen, (C₁ -C₆)-alkyl or (C₁ -C₄)-alkoxy-(C₁ -C₆)-alkyl, preferably R⁴ and R^(4') are hydrogen, (C₁ -C₈)-alkyl or methoxyethyl, particularly preferably hydrogen, (C₁ -C₄)-alkyl or methoxyethyl or R⁴ and R^(4'), together with the nitrogen atom carrying them, can also form a 5 to 6-membered heterocyclic ring which can additionally contain a further heteroatom from the series consisting of O, S and N;

b) complete or partial replacement of the 3'- or 5'-phosphoric acid diester bridges by "dephospho" bridges (see, for example, Uhlmann and Peyman in "Methods in Molecular Biology", Vol. 20, "Protocols for Oligonucleotides and Analogs", S. Agrawal, Ed., Humana Press, Totowa 1993, Chapter 16, 355ff), for example by formacetal, 3'-thioformacetal, methylhydroxylamine, oxime, methylenedimethylhydrazo, dimethylenesulfone or silyl groups;

c) complete or partial replacement of the sugar phosphate backbone, for example by "morpholinonucleoside" oligomers (E. P. Stirchak et al., Nucleic Acids Res. 17 (1989) 6129) or "PNAs" (P. E. Nielsen et al, Bioconj. Chem. (1994) 3), or PNA-DNA hybrids such as described, for example, in DE-P 44 08 528.1 and EP-A 0 672 677;

d) complete or partial replacement of the β-D-2'-deoxyribose units, for example by α-D-2'-deoxyribose, L-2'-deoxyribose, 2'-F-2'-deoxyribose, 2'-O-(C₁ -C₆)alkyl- ribose, 2'-O-(C₂ -C₆)alkenylribose, 2'-NH₂ -2'-deoxyribose, β-D-xylofuranose, α-arabinofuranose, 2,4-dideoxy-β-D-erythrohexopyranose, and carbocyclic (e.g. Froehler, J.Am.Chem.Soc. 114 (1992) 8320) and open-chain sugar analogs (e.g. Vandendriessche et al., Tetrahedron 49 (1993) 7223) or bicyclo sugar analogs (e.g. M. Tarkov et al., Helv. Chim. Acta 76 (1993) 481);

e) complete or partial replacement of the natural nucleoside bases, for example by 5-(hydroxymethyl)uracil, 5-aminouracil, pseudouracil, dihydrouracil, 5-(C₂ -C₆)-alkynyluracil (for example described in Gutierrez et al., J. Am. Chem. Soc. 116 (1994) 540 or Sagi et al., Tetrahedron Lett. 34 (1993) 2191), 5-(C₁ -C₆)-alkylcytosine, 5-(C₂ -C₆)-alkenylcytosine, 5-(C₂ -C₆)-alkynylcytosine (Gutierrez et al., J. Am. Chem. Soc. 116 (1994) 540 or Sagi et al., Tetrahedron Lett. 34 (1993) 2191), 5-fluorouracil, 5-fluorocytosine, 5-chlorouracil, 5-chlorocytosine, 5-bromouracil, 5-bromocytosine or 7-deaza-7-substituted purines (for example described in Seela, Nucl. Acids Res. 20 (1992)2297); Heterocycles 34 (1992) 229).

Q and Q' can also be conjugates which favorably affect the properties of antisense oligonucleotides or of triple helix-forming oligonucleotides (such as, for example, cell penetration, nuclease degradation, affinity for the target RNA/DNA, pharmacokinetics) or serve as a label of a DNA probe or during the hybridization of the oligonucleotide analog to the target nucleic acid, attacking the target nucleic acid through binding or crosslinking. Examples of these are conjugates with polylysine, with intercalators such as pyrene, acridine, phenazine, phenanthridine, with fluorescent compounds such as fluorescein, with crosslinkers such as psoralen, azidoproflavine, with lipophilic molecules such as (C₁₂ -C₂₀)-alkyl, with lipids such as 1,2-dihexadecyl-rac-glycerol, with steroids such as cholesterol or testosterone, with vitamins such as vitamin E, with poly- or oligoethylene glycol, with (C₁₂ -C₁₈)-alkyl phosphate diesters, with --O--CH₂ --CH(OH)--O-(C₁₂ -C₁₈)-alkyl. Preferred conjugates are those with lipophilic molecules such as (C₁₂ -C₂₀)-alkyl, with steroids such as cholesterol or testosterone, with poly- or oligoethylene glycol, with vitamin E, with intercalators such as pyrene, with (C₁₄ -C₁₈)-alkylphosphate diesters or with --O--CH₂ --CH(OH)--O-(C₁₂ -C₁₆)-alkyl.

The preparation of oligonucleotide conjugates of this type is known to the person skilled in the art (see, for example, Uhlmann & Peyman, Chem. Rev. 90 (1990) 543; M. Manoharan in "Antisense Research and Applications", Crooke and Lebleu, Eds., CRC Press, Boca Raton, 1993, Chapter 17, p. 303ff and EP-A 0 552 766). Furthermore, the oligonucleotides can carry 3'-3'-and 5'-5'-inversions on the 3' or on the 5'-end (described, for example, in M. Koga et al., J. Org. Chem. 56 (1991) 3757).

Aromatic groups are, for example, phenyl, naphthyl, pyrenyl, anthracenyl, phenanthryl, biphenyl, binaphthyl, tetracenyl, pentacenyl, hexacenyl, triphenylenyl, chrysenyl or benzopyrenyl.

Heterocyclic groups are understood as meaning, for example, chromanyl, chromenylium-1-yl, furanyl, isochromanyl, isochromenyl, isoquinolyl, piperazinyl, quinolinyl, pyridinyl, pyrrolidinyl, imidazolyl, tetrahydrofuranyl, aziridinyl, oxiranyl, thiophenyl, pyrimidinyl, thiolanyl, thiazolyl, azepinyl, pyrrolyl, tetrahydropyrrolyl, benzofuranyl, indolyl, isoindolyl, isatinyl, dioxindolyl, indoxylyl, coumarinyl, coumaronyl, carbazolyl, pyrazolyl, pyrrolyl, indazolyl, oxazolyl, isoxazolyl, thiazolyl, 1,2,4-triazolyl, 1,2,3-triazolyl, tetrazolyl, pentazolyl, piperidinyl, pyridazinyl, phenazinyl, phenoxazinyl, pyenothiazinyl, morpholinyl, thiazinyl, benzodiazepinyl, purinyl, xanthinyl, hypoxanthinyl, theophyllinyl, theobrominyl, caffeinyl, pteridinyl, pterinyl, pteridinyl, alloxazinyl and nortropinyl.

Natural nucleobases are understood as meaning, for example, uracil, cytosine, 5-methyluracil, adenine and guanine and unnatural nucleobases are understood as meaning, for example, 5-nitroindole, 5-(hydroxymethyl)-uracil, 5-aminouracil, pseudouracil, dihydrouracil, 5-(C₁ -C₆)-alkyluracil, 5-(C₂ -C₆)-alkenyluracil, 5-(C₃ -C₆)-alkynyluracil, 5-(C₁ -C₆)-alkylcytosine, 5-(C₂ -C₆)-alkenylcytosine, 5-(C₃ -C₆)-alkynylcytosine, 5-fluorouracil, 5-fluorocytosine, 5-chlorouracil, 5-chlorocytosine, 5-bromouracil, 5-bromocytosine and 7-deaza-7-substituted purines, such as 7-deaza-7-(C₃ -C₇)-alkynylguanine, 7-deaza-7-(C₃ -C₇)-alkynyladenine, 7-deaza-7-(C₂ -C₇)-alkenylguanine, 7-deaza-7-(C₂ -C₇)-alkenyladeine, 7-deaza-7-(C₁ -C₇)-alkylguanine, 7-deaza-7-(C₁ -C₇)-alkyladenine, 7-deaza-7-bromoguanine and 7-deaza-7-bromoadenine.

Preferably, unnatural nucleobases are 5-(C₁ -C₆)-alkyluracil, 5-(C₂ -C₆)-alkenyluracil, 5-(C₃ -C₆)-alkynyluracil, 5-(C₁ -C₆)-alkylcytosine, 5-(C₂ -C₆)-alkenylcytosine, 5-(C₃ -C₆)-alkynylcytosine, 5-chlorocytosine, 5-bromo-uracil, 5-bromocytosine or 7-deaza-7-substituted purines such as 7-deaza-7-(C₃ -C₇)-alkynylguanine, 7-deaza-7-(C₃ -C₇)-alkynyladenine, 7-deaza-7-(C₂ -C₇)-alkenylguanine, 7-deaza-7-(C₂ -C₇)-alkenyladenine, 7-deaza-7-(C₂ -C₇)-alkenyladeine, 7-deaza-7-(C₁ -C₇)-alkylguanine, 7-deaza-7-(C₁ -C₇)-alkyladenine, 7-deaza-7-bromoguanine and 7-deaza-7-bromoadenine, particularly preferably 5-(C₃ -C₆)-alkyluracil, 5-(C₂ -C₆)-alkenyl-uracil, 5-(C₃ -C₆)-alkynyluracil, 5-(C₁ -C₆)-alkylcytosine 5-(C₂ -C₆)-alkenylcytosine, 5-(C₃ -C₆)-alkynylcytosine or 7-deaza-7-substituted purines, and very particularly preferably 5-pentynylcytosine, 5-hexynyluracil, 5-hexynylcytosine, 7-deaza-7-propynylguanine, 7-deaza-7-propynylcytosine, 7-deaza-7-methylguanine, 7-deaza-7-methyladenine, 7-deaza-7-propynyladenine, 7-deaza-7-bromoguanine, 7-deaza-7-bromoadenine.

Reporter ligands are, for example, fluorescein, biotin, acridine, phenanthroline, phenanthridine and eosin.

Among D- or L-amino acids, if not stated otherwise, particularly the following may be mentioned (cf. Schroder, Lubke, Peptides, Volume 1, New York 1965, pages XXII-XXIII; Houben-Weyl, Methoden der Organischen Chemie, [Methods of Organic Chemistry] Volume XV/1 and 2, Stuttgart 1974):

Aad, Abu, γAbu, ABz, 2ABz, εAca, Ach, Acp, Adpd, Ahb, Aib, βAib, Ala, βAla, ΔAla, Alg, All, Ama, Amt, Ape, Apm, Apr, Arg, Asn, Asp, Asu, Aze, Azi, Bai, Bph, Can, Cit, Cys, Cyta, Daad, Dab, Dadd, Dap, Dapm, Dasu, Djen, Dpa, Dtc, Fel, Gln, Glu, Gly, Guv, hAla, hArg, hCys, hGln, hGlu, His, hlle, hLeu, hLys, hMet, hPhe, hPro, hSer, hThr, hTrp, hTyr, Hyl, Hyp, 3Hyp, Ile, Ise, Iva, Kyn, Lant, Lcn, Leu, Lsg, Lys, βLys, ΔLys, Met, Mim, Min, hArg, Nle, Nva, Oly, Orn, Pan, Pec, Pen, Phe, Phg, Pic, Pro, ΔPro, Pse, Pya, Pyr, Pza, Qin, Ros, Sar, Sec, Sem, Ser, Thi, βThi, Thr, Thy, Thx, Tia, Tle, Tly, Trp, Trta, Tyr, Val etc., whose abbreviations without a stereo- descriptor stand for the radical in the L-form, and cyclic amino acids, such as pyrrolidine-2-carboxylic acid; piperidine-2-carboxylic acid; 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid; decahydroisoquinoline-3-carboxylic acid; octahydroindole-2-carboxylic acid; decahydroquinoline-2-carboxylic acid; octahydrocyclopenta[b]pyrrole-2-carboxylic acid; 2-azabicyclo[2.2.2]octane-3-carboxylic acid; 2-azabicyclo[2.2.1]heptane-3-carboxylic acid; 2-azabicyclo[3.1.0]hexane-3-carboxylic acid; 2-azaspiro[4.4]nonane-3-carboxylic acid; 2-azaspiro[4.5]decane-3-carboxylic acid; spiro[(bicyclo[2.2.1]heptane)-2,3-pyrrolidine-5-carboxylic acid]; spiro[(bicyclo[2.2.2]octane)-2,3-pyrrolidine-5-carboxylic acid]; 2-azatricyclo[4.3.0.1⁶.9 ]decane-3-carboxylic acid; decahydrocyclohepta[b]pyrrole-2-carboxylic acid; decahydrocycloocta[b]pyrrole-2-carboxylic acid; octahydrocyclopenta[c]pyrrole-2-carboxylic acid; octahydroisoindole-1-carboxylic acid; 2,3,3a,4,6a-hexahydrocyclopenta[b]pyrrole-2-carboxylic acid; 2,3,3a,4,5,7a-hexahydroindole-2-carboxylic acid; tetrahydrothiazole-4-carboxylic acid; isoxazolidine-3-carboxylic acid; pyrazolidine-3-carboxylic acid; hydroxypyrrolidine-2-carboxylic acid; all of which can be optionally substituted with: ##STR4##

U.S. Pat. Nos. 4,344,949, 4,374,847and 4,350,704, and EP-A 29 488, EP-A 31 741, EP-A 46 953, EP-A 49 605, EP-A 49 658, EP-A 50 800, EP-A 51 020, EP-A 52 870, EP-A 79 022, EP-A 84 164, EP-A 89 637, EP-A 90 341, EP-A 90 362, EP-A 105 102, EP-A 109 020, EP-A 111 873, EP-A 271 865 and EP-A 344 682 describe cyclic amino acids.

In formula I even when n is greater than 1, the substitutions can be the same or different from each other.

Alkyl and radicals derived therefrom such as alkoxy and alkylthio can be branched, unbranched or cyclic, saturated or mono- or polyunsaturated.

Preferred compounds of the formula I are those wherein

n is a number from zero to 50;

B independently of one another is a natural nucleobase or an unnatural nucleobase;

L is N;

A is a group of the formula IIB, in which

r=1 and s is zero, and R², R³ ═H and Y'=O and M is a single bond;

D and G each independently represent CHR⁵ ;

R⁵ is hydrogen;

X is --O--;

Y is ═O;

Z is hydroxyl, methoxy, ethoxy, (4-nitrophenyl)ethoxy, propoxy, isopropoxy, butoxy, pentoxy, phenoxy or allyloxy;

Q and Q' independently of one another are hydrogen, R⁸ or oligonucleotides unmodified or modified, as follows:

a) the 3'- and/or 5'-phosphoric acid diester bridges are completely or partially replaced by phosphorothioate, phosphorodithioate, NR⁴ R^(4') -phosphoramidate, N3'-P5'-phosphoramidate (for example described in Gryaznov et al., J. Am. Chem. Soc. 116 (1994) 3143), phosphate O-methyl ester, phosphate O-ethyl ester, phosphate O-isopropyl ester, methylphosphonate or phenylphosphonate bridges;

b) one, two or three 3'- or 5'-phosphoric acid diester bridges in the pyrimidine positions and at the 5'-end and/or at the 3'-end are replaced by formacetals and/or 3'-thioformacetals;

c) the sugar phosphate backbone is completely or partially replaced by "PNAs" or PNA-DNA hybrids;

d) the β-D-2'-deoxyribose units are completely or partially replaced by 2'-F-2'-deoxyribose, 2'-O-(C₁ -C₆)-alkylribose, 2'-O-(C₂ -C₆)alkenylribose or 2'-NH₂ -2'-deoxyribose;

e) the natural nucleoside bases are completely or partially replaced by 5-(C₁ -C₆)-alkyluracil, 5-(C₂ -C₆)-alkenyluracil, 5-(C₂ -C₆)-alkynyluracil, 5-(C₁ -C₆)-alkylcytosine, 5-(C₂ -C₆)-alkenylcytosine, 5-(C₂ -C₆)-alkynylcytosine, 5-fluorouracil, 5-fluorocytosine, 5-chlorouracil, 5-chlorocytosine, 5-bromouracil, 5-bromocytosine, 7-deaza-7-deaza-7-(C₂ -C₇)-alkynylguanine, 7-deaza-7-(C₂ -C₇)-alkynyladenine, 7-deaza-7-(C₂ -C₇)-alkenylguanine, 7-deaza-7-(C₂ -C₇)-alkenyladenine, 7-deaza-7-(C₁ -C₇)-alkylguanine, 7-deaza-7-(C₁ -C₇)-alkyladenine, 7-deaza-7-bromoguanine, 7-deaza-7-bromoadenine.

Particularly preferred compounds of the formula I are those in which

n is a number from 0 to 30;

Q and Q' independently of one another are hydrogen, R⁸, in which R⁸ is H, (C₁ -C₆)-alkyl, phenyl or 2-(4-nitrophenyl)ethyl, or are oligonucleotides which can be unmodified or modified as follows:

a) the 3'-and/or 5'-phosphoric acid diester bridges are completely or partially replaced by phosphorothioate, phosphorodithioate or methylphosphonate bridges;

b) one, two or three 3'-or 5'-phosphoric acid diester bridges are replaced at the 5'-and at the 3'-end;

c) the sugar phosphate backbone is completely or partially replaced by "PNAs" or PNA-DNA hybrids;

d) the β-D-2'-deoxyribose units are completely or partially replaced by 2'-F-2'-deoxyribose, 2'-O-(C₁ -C₄)-alkylribose, 2'-O-(C₂ -C₄)alkenylribose or 2'-NH₂ -2'-deoxyribose;

e) the natural nucleoside bases are completely or partially replaced by 5-(C₃ -C₆)-alkyluracil, 5-(C₂ -C₆)-alkenyluracil, 5-(C₂ -C₆)-alkynyluracil, 5-(C₂ -C₆)-alkylcytosine, 5-(C₂ -C₆)-alkenylcytosine, 5-(C₂ -C₆)-alkynylcytosine, 7-deaza-7-(C₂ -C₇)-alkynylguanine, 7-deaza-7-(C₂ -C₇)-alkynyladenine, 7-deaza-7-(C₂ -C₇)-alkenylguanine, 7-deaza-7-(C₂ -C₇)-alkenyladenine, 7-deaza-7-(C₁ -C₇)-alkylguanine, 7-deaza-7-(C₁ -C₇)-alkyladenine, 7-deaza-7-bromoguanine, 7-deaza-7-bromoadenine.

Very particularly preferred compounds of the formula I are those in which

n is a number from 0 to 25;

B independently of one another is a natural nucleobase;

Z is hydroxyl, ethoxy, (4-nitrophenyl)ethoxy or phenoxy;

Q and Q' independently of one another is hydrogen, R⁸, in which R⁸ is H, (C₁ -C₆)-alkyl, phenyl or 2-(4-nitrophenyl)ethyl, or are oligonucleotides which can be unmodified or modified as follows,

a) the 3'-and/or 5'-phosphoric acid diester bridges are completely or partially replaced by phosphorothioate bridges;

c) the sugar phosphate backbone is completely or partially replaced by "PNAs" or PNA-DNA hybrids;

d) the β-D-2'-deoxyribose units are completely or partially replaced by 2'-O-methyl, 2'-O-allyl or 2'-O-butylribose; or

e) the natural nucleoside bases are completely or partially replaced by 5-hexynylcytosine, 5-hexynyluracil, 5-hexynylcytosine, 7-deaza-7-propynylguanine, 7-deaza-7-propynyladenine, 7-deaza-7-methylguanine, 7-deaza-7-methyladenine, 7-deaza-7-bromoguanine, 7-deaza-7-bromoadenine.

The invention further relates to compounds of the formula I in which Q and Q' are linked, i.e. form a cyclic molecule, where the possibility should still apply that Q and Q' together afford a single bond. The synthesis of such compounds can be carried out analogously to described processes, for example Gao et al., Nucl. Acids Res. 23 (1995) 2025, or Wang and Kool, Nucl. Acids Res. 22 (1994) 2326.

The invention further relates to oligonucleotides or modified oligonucleotides, for example PNAs, in which compounds of the formula I are incorporated at the 3'-end or at the 5'-end or at the 5'- and at the 3'-end.

The linkage of the oligonucleotides with the compounds of the formula I is preferably carried out via the 5'-or 3'-hydroxyl group of the nucleotide units, likewise via a phosphonic acid monoester bond. The linkage with oligonucleotides is illustrated by way of example in the formulae XVIII and XIX. ##STR5##

R¹⁷ is H, OH, F, 2'-O-(C₁ -C₆)-alkyl or 2'-O-(C₂ -C₆)-alkenyl, preferably H or methoxy or O-allyl, particularly preferably H. All other variables are illustrated above.

Formula XX and formula XXI, in which the variables have the above meaning, illustrate by way of example the linkage with PNAs. ##STR6##

The combinations of the compounds according to the invention utilizing (abbreviated PMENA) oligonucleotides or modified oligonucleotides, will be schematically illustrated again (OLIGO is unmodified or modified oligonucleotides) for example PNAs or other modifications, as are described above:

Examples of such combinations are:

5'-OLIGO-PMENA

5'-PMENA-OLIGO

5'-OLIGO-PMENA-OLIGO

5'-OLIGO-(PMENA-OLIGO)_(a) (a=1-20)

5'-PMENA-OLIGO-PMENA

5'-PMENA-(OLIGO-PMENA)_(a) (a=1-20)

The synthesis of these combined compounds is carried out in such a way that, according to the molecule, the synthesis of the PMENA units, which is described in the following, is begun first, which are then coupled with the oligonucleotide units. In this process, the oligonucleotides are coupled as monomer units or by block condensation by solid-phase synthesis or by solution synthesis by methods known to the person skilled in the art (Sonveaux, Bioorganic Chemistry 14 (1986) 274ff). The condensations are alternatively carried out by the amidite method, the H-phosphonate method or the phosphorotriester process (Sonveaux, Bioorganic Chemistry 14 (1986) 274ff). If, conversely, PMENA units are coupled to OLIGO units, this is preferably carried out by the method described in f₁) below. Conjugation with PNA units is carried out in the same manner or, if (monomeric or oligomeric) PNA units are coupled to PMENA units, with the methods of peptide synthesis or of ester synthesis known to the person skilled in the art. These combinations can be made by means apparent to those skilled in the art in view of the present specification.

The invention furthermore relates to a compound having one of the formulae:

5'-Q¹¹ -OLIGO-(PMENA-OLIGO)a-Q¹² ;

5'-Q¹³ -PMENA-OLIGO-PMENA-Q¹⁴ ;

5'-Q¹⁵ -PMENA-(OLIGO-PMENA)a-Q¹⁶ ; or

5'-OLIGO-(PMENA-OLIGO)a;

wherein a is 1-20, OLIGO represents an unmodified or modified oligonucleotide, and PMENA represents a compound of formula I': ##STR7## in which B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl, (C₆ 14 C₂₀)-aryl-(C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkythio, an aromatic group or a heterocyclic group, wherein alkyl, aryl, aromatic or heterocyclic group is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, --C(O)OH, oxo, --C(O)OR⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₆)-alkoxyalkyl, --S(O)_(m) R⁸, --(C₁ -C₆) --alkyl-S(O)_(m) R⁸, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NT⁹ R¹⁰, or --NR⁹ C(═O)NR⁹ R¹⁰,

B independently of one another is a natural nucleobase, an unnatural nucleobase or a reporter ligand;

A-B is a D--or L-amino acid condensed on via the carboxyl group or peptides consisting of amino acids having a length of up to 5 amino acid residues,

L independently of one another is N or R¹ N⁺, and

R¹ is hydrogen or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆) -alkoxy, (C₁ -C₆)-alkylthio or amino;

A independently of one another is a single bond, a methylene group or a group of formula IIa or IIb; ##STR8## Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above;

M is a single bond, --O--, --S-- or --NR¹ --, where R¹ is as defined above;

R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio;

p and q independently of one another are zero to 5;

r and s independently of one another are zero to 5;

D and G each independently represent Cr⁵ R⁶ which can be the same or different;

R⁵ and R⁶ independently of one another are hydrogen, (C₁ -C₆ -alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀) -aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, wherein alkyl and aryl are optionally substituted by SR¹ or NR¹ R^(1'), where R¹ is as defined above and R^(1') independently of R¹ has the same meaning as R¹ ;

X is --O--, --S-- or --NR¹ --, in which R¹ is as defined above;

Y is ═O or ═S;

Z is --OR⁸, --NR⁹ R¹⁰ or X'Q', where X'is defined as X and Q' is hydrogen, R⁸, modified or unmodified oligonucleotides or conjugates which a) favorably affect the properties of antisense oligonucleotide, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a lable of a DNA probe, or d) during the hycridization of the oligonucleotides analog to the target nucleic acid, attack the target nucleic acid with binding or crosslinking;

R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ --C₁₈)-alkynly, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, wherein alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and wherein aryl is optionally substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰ ;

R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkyoxy, F, Cl or Br; or R⁹ and R¹⁰ form a 4 to 7-membered ring together with the N atom in --NR⁹ R¹⁰ ;

and wherein Q¹³ and Q¹⁴ either both represent hydrogen or together form a bond in a cyclic molecule; Q¹⁵ and Q¹⁶ either both represent hydrogen or together form a bond in a cyclic molecule; and Q¹¹ and Q¹² form a singel bond in a cyclic molecule.

The invention furthermore relates to a process for the preparation of compounds of the formula I, which comprises

a₁) reacting a compound of formula III ##STR9## in which

D, G, L and X have the abovementioned meanings and

S¹ is a suitable protective group, such as dimethoxytrityl, monomethoxytrityl, trityl, pixyl, tert-butoxycarbonyl or fluorenylmethoxycarbonyl, preferably monomethoxytrityl or tert-butoxycarbonyl,

with a compound of formula IV ##STR10## in which

R⁵ and R⁶ have the abovementioned means,

in a suitable organic solvent, for example in methanol, ethanol, isopropanol, butanol, acetonitrile, dichloromethane (DCM), chloroform, benzene, dimethylformamide (DMF), dimethyl sulfoxide (DMSO), diethyl ether, ethyl acetate (EA), tetrahydrofuran (THF), N-methylpyrrolidone, petroleum ether, xylene or toluene or mixtures of suitable solvents, preferably in methanol or ethanol, at temperatures sufficient to form (e.g. from 0° C. to 100° C., preferably at 10 to 50° C.) compounds of formula Va or Vb ##STR11## where, in the choice of the reaction conditions which are known to the person skilled in the art (e.g. in S. R. Sandler, W. Karo "Organic Functional Group Preparations", Vol. II, Second Edition, Academic Press, London, 1986, Chapter 12 ("Imines")), care is to be taken that they are compatible with the protective group S¹, i.e. if, for example, an acid-labile protective group such as the monomethoxytrityl protective group is chosen, no acid should be added during the reaction,

b₁) reacting compounds of the formula Va or Vb with compounds of the formula VIa or VIb, preferably with compounds of the formula VIa ##STR12## in which

Y is as defined above,

X' and X" independently of one another have the same meaning as X defined above,

S² and S³ independently of one another are protective groups such as methyl, ethyl, phenyl, 2-chlorophenyl, 2,5-dichlorophenyl, 2,4-dichlorophenyl, 4-nitrophenyl, 4-methoxyphenyl, 2-cyanoethyl, 2-(4-nitrophenyl)ethyl, allyl, benzyl, 2,2,2-trichloro-1,1-dimethylethyl, 4-methoxybenzyl, 2,2,2-trichloroethyl, 8-hydroxyquinoline or other phosphate protective groups, such as are known to the person skilled in the art (Sonveaux, Bioorganic Chemistry 14 (1986) 274 ff), but preferably methyl, ethyl, phenyl, 2-(4-nitrophenyl)ethyl, allyl or 2,2,2-trichloroethyl, and

L¹ is a leaving group, preferably (C₁ -C₄)-alkyl,

in a suitable organic solvent, for example in methanol, ethanol, isopropanol, butanol, acetonitrile, benzene, DMF, DMSO, DCM, EA, chloroform, diethyl ether, THF, N-methylpyrrolidone, petroleum ether, xylene or toluene or mixtures of suitable solvents, preferably in THF, at temperatures sufficient to form a compound of formula VII, e.g. from 0° C. to 100° C., preferably at 50 to 80° C., if appropriate with optional addition of bases, such as tri-(C₁ -C₆ -alkylamine, N-alkylmorpholine, pyridine, N,N-diemthylaminopyridine, butyllithium, lithium diisopropylamide (LDA), sodium hydride, sodium amide, potassium carbonate, cesium carbonate, potassium tert-butoxide or complex bases such as sodium amide-R¹¹ ONa, where R¹¹ is (C₂ -C₆)-alkyl of CH₃ CH₂ --O--CH₂ CH₃, or uncharged, peralkylated polyaminophosphazene bases (Schwesinger, Nachr. Chem. Techn. Lab. 38 (1990) 1214; Angew. Chem. 99 (1987) 1212), but preferably without addition of base.

Formula VII has the following formula: ##STR13## in which

D, G, L, R⁵, R⁶, S¹, S², S³, X, X', X" and Y are as defined above;

c₁) reacting a compound of formula VII with a compound of formula VIII ##STR14## whose synthesis is described, for example, in Dueholm et al., J. Org. Chem. 59 (1994) 5767 and

in which

A has the abovementioned meaning.

B^(PR) has the same meaning as B, but is optionally present in protected form, i.e. if B is a natural or unnatural nucleobase, B^(PR) is the nucleobase whose amino or hydroxyl group's are protected by suitable known protective groups, such as the para-nitrophenylethyl group, the benzoyl group, the allyl group and the para-(t-butyl)benzoyl group for the hydroxyl group and the acetyl, benzoyl, para-(t-butyl)benzoyl, para-(methoxy)benzoyl group, para-nitrophenylethoxycarbonyl group, isobutyryl group, para-(t-butyl)phenylacetyl group, N,N-dimethylformamidino group, fluorenylmethyloxycarbonyl group, benzyloxycarbonyl group or phenoxyacetyl group for the amino group or other protective groups customary for nucleobases in oligonucleotide chemistry (Sonveaux, Bioorganic Chemistry 14 (1986) 274ff; Beaucage, Tetrahedron 49 (1993) 2223ff), preferably the following may be mentioned for B^(PR) : ##STR15## in which

R¹² is hydrogen, 1-propynyl, 1-butynyl, 1-pentynyl or 1-hexynyl, in particular hydrogen, 1-propynyl or 1-hexynyl; and

R¹³ is hydrogen, diphenylcarbamoyl or 2-(4-nitrophenyl)-ethyl and

R¹⁴ is acetyl, benzoyl, para-(t-butyl)benzoyl, para-(methoxy)benzoyl, para-nitrophenylethyloxycarbonyl, isobutyryl, para-(t-butyl)phenylacetyl, benzyloxycarbonyl or phenoxyacetyl, and

L² is a leaving group known to the person skilled in the art, such as Cl, Br, O-SO₂ methyl, O-SO₂ trifluoromethyl, O-tosylate or O--C₆ F₅ or, if A has the meaning of formula IIB, can also be OH;

in a suitable organic solvent, for example in acetonitrile, benzene, DMF, DMSO, DCM, EA, chloroform, diethyl ether, tetramethylurea, THF, N-methylpyrrolidone, petroleum ether, xylene or toluene or mixtures of suitable solvents, preferably in DMF, at temperatures sufficient to form a compound of the formula IX, e.g. from -20° C. to 100° C., more preferably at 0 to 50° C., if appropriate with optional addition of bases, such as tri-(C₁ -C₆)-alkylamine, N-alkylmorpholine, pyridine, N,N-dimethylaminopyridine, butyllithium, lithium diisopropylamide (LDA), sodium hydride, sodium amide, potassium carbonate, cesium carbonate, potassium tert-butoxide or complex bases such as sodium amide-R¹¹ ONa, where R is (C₂ -C₆)-alkyl or CH₃ CH₂ --O--CH₂ CH₃ or the bases are unchanged, peralkylated polyamino-phosphazene bases (Schwesinger, Nachr. Chem. Techn. Lab. 38 (1990) 1214; Angew. Chem. 99 (1987) 1212), and if A is formula IIb and L² is OH, preferably with addition of triethylamine, diisopropylethylamine or N-ethylmorpholine or without addition of base and with addition of a coupling reagent customary for the coupling of peptide bonds.

Formula IX has the following formula: ##STR16## in which

A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², S³, X, X', X" and Y are as defined above:

d₁) removing the protective group S₃ from compounds of the formula IX by known processes (e.g. Greene, Wuts, Protective Groups in Organic Synthesis, J. Wiley & Sons, New York 1991). For example, for compounds of the formula IX, in which S² and S³ are 2-(4-nitrophenyl)ethyl, by treatment with 0.1M 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in pyridine or acetonitrile at room temperature or for compounds of the formula IX in which S² and S³ are phenyl or ethyl, by treatment with an aqueous ammonia or for compounds of the formula IX in which S² is 2-(4-nitrophenyl)ethyl and S³ is allyl, by treatment with Pd[P(C₆ H₅)₃ ]₄ and triphenylphosphine in DCM (Hayakawa et al., J. Org. Chem. 58 (1993) 5551); or for compounds of the formula IX in which S² is 2-(4-nitrophenyl)ethyl and S³ is ally, by treatment with 0.5M DBU in pyridine or acetonitrile or for compounds of the formula IX in which S² is 2-cyanoethyl and S³ is allyl, by treatment with triethylamine in pyridine, or for compounds of the formula IX in which S² is 2-(4-nitrophenyl)ethyl and S³ is 2,2,2-trichloro-1,1-dimethylethyl, by treatment with tributylphosphine.

compounds of the formula X being obtained ##STR17## in which

A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above;

e₁) removing the protective group S₁ from compounds of the formula IX by known processes (e.g. Greene, Wuts, Protective Groups in Organic Synthesis, J. Wiley & Sons, New York 1991, Sonveaux, Bioorganic Chemistry 14 (1986) 274 ff), thus, for example, the monomethoxytrityl protective group is removed by treatment with acid, for example by treatment with 80% acetic acid, with 1-4% dichloroacetic acid in methylene chloride or chloroform, with 2% p-toluenesulfonic acid in DCM/methanol or by treatment with 1% trifluoroacetic acid in chloroform,

compounds of the formula XI being obtained ##STR18## in which

A, B^(PR), D, G, L, R⁵, R⁶, S², S³, X, X', X" and Y are as defined above;

f₁) reacting compounds of the formula XI with compounds of the formula X according to the "phosphotriester process" known from oligonucleotide chemistry (Sonveaux, Bioorganic Chemistry 14 (1986) 2744ff, Reese, J. Chem. Soc. Perkin Trans. 1993, 2291ff) in a suitable organic solvent, such as acetonitrile, benzene, DMF, DMSO, DCM, EA, chloroform, diethyl ether, tetramethylurea, THF, N-methylpyrrolidone, petroleum ether, xylene or toluene or mixtures of suitable solvents, preferably in pyridine, at temperatures from -20° C. to 100° C., more preferably at 0 to 50° C., with addition of a coupling reagent, such as 6-nitrobenzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (NBOP, Hashmi, Nucleosides & Nucleotides 13 (1994) 1059), benzotriazole-1-yloxytris (dimethylamino)phosphonium hexafluorophosphate (BOP, B. Castro, J. R. Dormoy, G. Evin and C. Selve, Tetrahedron Lett. 1975, 1219-1222), benzotriazol-1-yloxytripyrrolidino)phosphonium hexafluorophosphate (PyBOP, J. Coste, D. Le-Nguyen and B. Castro, Tetrahedron Lett. 1990, 205-208), O-(7-aza)benzotriazol-1-yltetramethyluronium hexafluorophosphate (HATA, L. Carpino, J. Am. Chem. Soc. 1993, 115, 4397), N,N-bis[2-oxo-3-oxazolidinyl]diaminophosphoryl chloride (Katti, Tetrahedron Lett. 26 (1985) 2547), 2-chloro-5,5-dimethyl-2-oxo-1,3,2-dioxaphosphorinane (Stawinski, Nucl. Acids Res., Symp. Ser. 24, 1991, 229) or a compound of the formula XII ##STR19## in which

R¹⁵ is (C₆ -C₁₂)-aryl, optionally substituted one to four times by (C₁ -C₆)-alkyl, (C₁ -C₆)-alkoxy, nitro, chlorine or bromine and where one to 3 carbon atoms are optionally substituted by heteroatoms, preferably nitrogen, i.e. for example phenyl, tolyl, 2,4,6-trimethylphenyl, 2,4,6-triisopropylphenyl, 2,3,5,6-tetramethylbenzene (Losse, Liebigs Ann. Chem. 1989, 19ff), 4-bromobenzene, 2-nitrobenzene, 4-nitrobenzene or 8-quinolyl, preferably 2,4,6-trimethylphenyl or 2,4,6-triisopropylphenyl, and

R¹⁶ is a leaving group such as chlorine, bromine, imidazole, triazole, 4-nitroimidazole, 1,2,3,4-tetrazole or 3-nitro-1,2,4-triazole.

preferably using a coupling reagent of the compound of the formula XII or BOP, PyBOP or HATU, optionally with addition of a catalyst (Reese, J. Chem. Soc, Perkin Trans. 1993, 2291ff), such as N-methylimidazole, pyridine-N-oxides such as 4-methoxypyridine-N-oxide or 4-ethoxypyridine-N-oxide, 4,6-dinitro-1-hydroxybenzotriazole, 1-hydroxyl-5-phenyltetrazole,1-hydroxy-5-(4-nitrophenyl)tetrazole, 3-nitro-1H-1,2,4-triazole, 5-(3-nitrophenyl)-1H-tetrazole, 5-(3,5-dinitrophenyl)-1H-tetrazole, 5-(1-methylimidazole-2-yl)methyl]-1H-tetrazole, 5-[(1-methylimidazole-2-yl)methyl]-1H-tetrazole or 1-hydroxy-4-nitro-6-(trifluoromethyl)benzotriazole, preferably with 4-ethoxypyridine-N-oxide or 4-methoxypyridine-N-oxide as a catalyst, where the preparation of the coupling reagents can be carried out in situ, or else carried out separately and the solution of the activated species (compound of formula (X) in combination with a coupling reagent) can be added in a suitable solvent.

to give compounds of the formula XIII ##STR20## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², S³, X, X', X" and Y are as defined abvoe;

g₁) starting from compounds of the formula XIII, repeating the steps e₁) and f₁) up to the desired chain length, compounds of the formula XIV resulting ##STR21## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², S³, X, X', X", Y and n are as defined above;

h₁) removing the protective groups S¹, S² and S³ and the protective groups on B^(PR) according to known processes (e.g. Greene, Wuts, Protective Groups in Organic Synthesis, J. Wiley & Sons, New York 1991),

i.e., for example, the protective group S¹ as described in step e₁), the protective groups S² or S³, if they are 2-(4-nitrophenyl)ethyl, by treatment with 0.5M 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in pyridine or acetonitrile at room temperature, if S² or S³ is phenyl, by treatment with aqueous ammonia, if S² or S³ is allyl, by treatment with Pd[P(C₆ H₅)₃ ]₄ and triphenylphosphine in DCM (Hayakawa et al., J. Org. Chem. 58 (1993) 5551), if S² or S³ is 2-cyanoethyl, by treatment with triethylamine in pyridine, or if S² or S³ is 2,2,2-trichloro-1,1-dimethylethyl, by treatment with tributylphosphine, and the protective groups on B^(PR), for example if R¹⁴ is para-nitrophenylethyloxycarbonyl, with 0.5M DMU in pyridine, if R¹⁴ is isobutyryl or benzoyl or para-methoxybenzoyl, with conc. NH₄ OH at 20 to 60° C. or, if R¹³ is 2-(4-nitrophenyl)ethyl, by treatment with 0.5M DBU in pyridine or acetonitrile, is preferred, if S¹ equals monomethoxytrityl and S² equals 2-(para-nitrophenyl)ethyl, preferably the monomethoxytrityl group is first removed as described in e₁), then S² is removed as described, then the remaining protective groups, for example on the nucleobases, are removed;

and optionally introducing the groups Q and Q' according to processes known to the person skilled in the art, (see, for example, Uhlmann & Peyman, Chem. Rev. 90 (1990) 543; M. Manoharan in "Antisense Research and Applications", Crooke and Lebleu, Eds., CRC Press, Boca Raton, 1993, Chapter 17, p.303ff; EP-A 0 552 766; S. Agrawal in Methods in Molecular Biology, Vol. 26, P. 93 ff, Humana Press, Totowa 1994), and optionally cyclizing the compounds obtained according to Wang, Nucl. Acids Res. 22 (1994) 2326, whereby compounds of the formula I result.

Alternatively, conjugates Q' can also be incorported into the monomer units of the formula XXII by prcoesses known to the person skilled in the art (J. March, "Advanced Organic Chemistry", Fourth Ed., J. Wiley & Sons, 1992), which are then incorporated into the compounds of the formula I according to the processes mentioned. ##STR22##

Compounds of the formula XXII can be prepared, for example, for Q'=alkyl, by reaction of compounds of the formula XXIII with compounds of the formula VIa or VIb and further reactions analogously to those described for the formulae Va and Vb. ##STR23##

Compounds of the formula XXII can also be prepared from compounds of the formula IX by removal of the protective group S¹ and introduction of the group Q' according to known processes (J. March, "Advanced Organic Chemistry", Fourth Ed., J. Wiley & Sons, 1992).

Alternatively, conjugates Q and Q" can also be incorporated into the monomer units of the formula XXIV by processes known to the person skilled in the art (J. March, "Advanced Organic Chemistry", Fourth Ed., J. Wiley & Sons, 1992), which are then incorporated into the compounds of the formula I according ot the processes mentioned. ##STR24##

Coupling reagents for the linkage of peptide bonds (see c₁)) are described, for example, in Houben-Weyl, Methoden der oganischen Chemie, [Methods of organic chemistry] Volume 15/2, Georg Thieme Verlag Stutgart 1974 and further reagents such as BOP (B. Castro, J. R. Dormoy, G. Evin and C. Selve, Tetrahedron Lett. 1975, 1219-122), PyBOP (J. Coste, D. Le-Nguyen and B. Castro, Tetrahedron Lett. 1990, 205-208), BroP (J. Coste, M.-N. Dufour, A. Pantaloni and B. Castro, Tetrahedron Lett. 1990, 669-672), PyBroP (J. Coste, E. Frerot, P. Jouin and B. Castro, Tetrahedron Lett. 1991, 1967-1970) and uronium reagents, such as HBTU (V. Dourtoglou, B. Gross, V. Lambropoulou, C. Zioudrou, Synthesis 1984, 572-574), TBTU, TPTU, TSTU, TNTU (R. Knorr, A. Trzeciak, W. Bannwarth and D. Gillessen, Tetrahedron Letters 1989, 1927-1930), TOTU (EP-A-O 460 446), HATU (L. A. Carpino, J. Am. Chem. Soc. 1993, 115, 4397-4398), HAPyU, TAPipU (A. Ehrlich, S. Rothemund, M. Brudel, M. Beyermann, L. A. Carpino and M. Bienert, Tetrahedron Lett. 1993, 4781-4784), BOI (K. Akaji, N. Kuriyama, T. Kimura, Y. Fujiwara and Y. Kiso, Tetrahedron Lett. 1992, 3177-3180) or acid chlorides or acid fluorides (L. A. Carpino, H. G. Chao, M. Beyermann and M. Bienert, J. Org. Chem., 56 (1991), 2635; J.-N. Bertho, A. Loffet, C. Pinel, F. Reuther and G. Sennyey in E. Giralt and D. Andreu (Eds.) Peptides 1990, Escom Science Publishers B. V. 1991, pp. 53-54; J. Green and K. Bradley, Tetrahedron 1993, 4141-4146), 2,4,6-mesitylenesulfonyl-3-nitro-1,2,4-triazolide (MSNT) (B. Blankemeyer-Menge, M. Nimitz and R. Frank, Tetrahedron Lett. 1990, 1701-1704), 2,5-diphenyl-2,3-dihydro-3-oxo-4-hydroxythiophene dioxide (TDO) (R. Kirstgen, R. C. Sheppard, W. Steglich, J. Chem. Soc. Chem. Commun. 1987, 1870-1871) or activated esters (D. Hudson, Peptide Res. 1990, 51-55) in the respective references.

The use of carbodiimides, e.g. dicyclohexylcarbodiimide or diisopropylcarbodiimide, is further preferred. Phosphonium reagents, such as PyBOP or PyBroP, uronium reagents, such as HBTU, TBTU, TPTU, TSTU, TNTU, TOTU or HATU and BOI are also preferably used.

In this case, the coupling can be carried out directly by addition of compounds of the formula VIII using the activating reagent and optionally with addition of additives such as 1-hydroxybenzotriazole (HOBt) (W. Konig, R. Geiger, Chem. Ber. 103, 788 (1970)) or 3-hydroxy-4-oxo-3,4-dihydrobenzotriazine (HOObt) (W. Konig, R. Geiger, Chem. Ber. 103, 2034 (1970)) or else the preactivation of the units as an activated ester can be carried out separately and the solution of the activated species in a suitable solvent can be added.

The invention furthermore relates to a process for the preparation of the compounds of the formula I, in which n is 1 to 100, which comprises, in the compounds of the formulae XV and XVI ##STR25## in which

A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², S³, X, X', X" and Y are as defined above,

o and p independently of one another are zero to 50, preferably zero to 20 and o+p+1=n;

a₂) in the compounds of the formula XV removing the protective group S¹ as described under e₁),

b₂) in the compounds of the formula XVI removing the protective group S³ as described under d₁) and

c₂) coupling the resulting compounds with one another as described under f₁), compounds of the formula XIV resulting ##STR26## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S³, X, X', X", Y and n are as defined above,

d₂) and reacting these as described under h₁) to give compounds of the formula I.

The invention furthermore relates to a process for the preparation of the compounds of the formula I, which comprises

a₃) coupling compounds of the formula X ##STR27## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above,

to a solid support via a SPACER according to known processes, to give compounds of the formula XVII, ##STR28## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above,

SS is a solid support suitable for solid-phase synthesis, such as aminopropyl-CPG (CPG=®Controlled Pore Glass) or ®Tentagel, and

SPACER is a group removable from the support after synthesis has taken place, such as is known to the person skilled in the art (Sonveaux, Bioorganic Chemistry 14 (1986) 274ff), for example the bis(hydroxyethyl)sulfonyl group, as is described in EP-A 0 552 766 or SPACER is bifunctional conjugate molecules Q, which are linked to the solid support via known removable groups, for example is nucleotides or oligonucleotides which are bound to the solid support via a succinic acid radical (Sonveaux, Bioorganic Chemistry 14 (1986) 274ff) or poly- or oligoethylene glycols which are bound to the solid support via a succinic acid radical (Jaschke, Tetrahedron Lett. 34 (1993) 301) or, for example, cholesterol derivatives which are bound to the solid support via a succinic acid radical (MacKellar, Nucl. Acids Res. 20 (1992) 3411);

b₃) removing the protective group S¹ from compounds of the formula XVII ##STR29## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², SS, SPACER, X, X', X" and Y are as defined above,

A variation of the above latter-described process for the preparation of a compound of formula I comprises

a₃) coupling a compound of formula X ##STR30## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above,

to a solid support (SS) via a SPACER to form a compound of formula XVII, ##STR31## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above,

SS is a solid support suitable for solid-phase synthesis, and

SPACER is a group removable from the support after synthesis has taken place, or SPACER is a bifunctional conjugate molecule Q linked to solid support via removable groups,

b₃) removing the protective group S¹ from the compound of formula XVII

c'₃) reacting the resulting compound with a compound of formula X ##STR32## in an organic solvent, with addition of a coupling reagent or a compound of formula XII ##STR33## in which R¹⁵ is (C₆ -C₁₂)-aryl, optionally substituted one to four times by (C₁ -C₆)-alkyl, (C₁ -C₆)- alkoxy, nitro, chlorine or bromine and where one to 3 ring carbon atoms are optionally substituted by heteroatoms, and

R¹⁶ is a leaving group,

optionally with addition of a catalyst, to form a compound of the formula XIII' ##STR34## d'₃) starting from the compound (XIII') resulting from said step c'₃) , repeating steps b₃) and c'₃) as necessary to form a compound of formula XIV'; ##STR35## e'₃) in any order, removing the protective groups on B^(pr) ; removing the protective group S¹ and optionally coupling conjugate Q'; removing the resulting compound of step d'₃) from the solid support and optionally coupling conjugate Q; removing the protective groups S² and optionally introducing Q", R⁸, R⁹ and R¹⁰,

in which

Q, Q', Q", R⁸, R⁹ and R¹⁰ are as defined above,

F'₃) optionally cyclizing, to form a compound of formula I.

as described under e₁);

c₃) reacting the resulting compound with compounds of the formula X ##STR36## in which A, B^(PR), D, G, L, R⁵, R⁶, S¹, S², X, X', X" and Y are as defined above,

as described under f₁);

d₃) repeating the steps b₃) and c₃) up to the desired chain length;

e₃) optionally coupling conjugates Q' by known processes (see, for example, Uhlmann & Peyman, Chem. Rev. 90 (1990) 543; M. Manoharan in "Antisense Research and Applications", Crooke and Lebleu, Eds., CRC Press, Boca Raton, 1993, Chapter 17, P.303ff; EP-A 0 552 766; S. Agrawal in "Methods in Molecular Biology", Vol. 26, P. 93ff, Humana Press, Totowa 1994);

f₃) removing the compounds produced in this way from the solid support by known proceses, for example the bis(hydroxyethyl)sulfonyl linkers, as described in EP-A 0 552 766, (HOE92/F012) by treatment with DBU, the succinic acid linker by treatment with aqueous ammonia and the protective groups as described in step h₁), where the removal of the protective groups can also be carried out before the cleavage from the support.

The compounds of the formula I are used as inhibitors of gene expression. The invention therefore further relates to the use of therapeutically active compounds according to the invention for the production of a pharmaceutical and to a process for the production of a pharmaceutical which comprises mixing the compounds according to the invention with a physiologically acceptable excipient and also, if appropriate, suitable additives and/or auxiliaries.

Therapeutically active compounds are understood in general as meaning those which, on account of the sequence of the units B which correspond to the nucleobases, carry out a function as analogs of antisense oligonucleotides, triple helix-forming oligonucleotides, aptamesr (RNA or DNA molecules which can bind to specific target molecules, e.g. proteins or receptors (e.g. L. C. Bock et al., Nature 1992, 355, 564) or ribozymes (catralytic RNA, see for example, Castanetto et al., Critical Rev. Eukar. Gene Expr. 1992, 2, 331), in particular as analogs of antisense oligonucleotides and triple helix-forming oligonucleotides.

Moreover, the present invention further relates to the use of the compounds according tothe invention as a diagnostic, for example for the detection of the presence or absence or the amount of a specific double-stranded or single-stranded nucleic acid molecule in a biological sample.

For use according to the invention, the compounds according to the invention generally have a length (n-1) of about 6-100, preferably of about 10-40, in particular of about 12-31 nucleotides. Otherwise, the preferred ranges, modifications or conjugations described above also apply here.

The pharmaceuticals of the present invention can be used, for example, for the treatment of illnesses which are caused by viruses, for example by HIV, SV-1, HSV-2, influenza, VSV, heptatitis B or papilloma viruses.a) against HIV, e.g.ACACCCAATTCTGAAAATGG SEQ ID NO:1AGGTCCCTGTTCGGGCGCCA SEQ ID NO:2GGTCCCTGTTCGGGCGCCA SEQ ID NO:26GTCGACACCCAATTCTGAAAATGGATAA SEQ ID NO:3GCTATGtCGACACCCAATTCTGAAA SEQ ID NO:4GTCGCTGTCTCCGCTTCTTCTTCCTG SEQ ID NO:5GTCTCCGCTTC-TICTTCCTGCCATAGG SEQ ID NO:6b) against HSV-1, e.g.GCGGGGCTCCATGGGGGTCG SEQ ID NO:7GGAGGATGCTGAGGAGG SEQ ID NO:28GGAGGATGCTGAGG SEQ ID NO:29CAGGAGGATGCTGAGGAGG SEQ ID NO:30

The pharmaceuticals of the present invention are also suitable, for example, for the treatment of cancer or of restenosis. For example, in this case sequences (base sequences) can be used which are directed against targets which are responsible for carcinogenesis or cancer growth. Such targets are, for example:

1) Nuclear oncoproteins such as c-myc, N-myc, c-myb, c-fos, c-fos/jun, PCNA, p120

2) Cytoplasmic/membrane-associated oncoproteins such as EJ-ras, c-Ha-ras, N-ras, rrg, bcl-2, cdc-2, c-raf-1, c-mos, c-src, c-abl

3) Cellular receptors such as EGF receptor, c-erbA, retinoid receptors, protein kinase regulatory subunits, c-fms

4) Cytokines, growth factors, extracellular matrix such as CSF-1, IL-6, IL-1a, IL-1b, IL-2, IL-5, bFGF, myeloblastin, fibronectin.

4) Cytokines, growth factors, extracellular matrix such as CSF-1, IL-6, IL-1a, IL-1b, IL-2, IL-4, bFGF, myeloblastin, fibronectin.

Sequences according to the invention (base sequences) which are active against targets of this type are, for example,a) against c-Ha-ras, e.g.CAGCTGCAACCCAGC SEQ ID NO:8c) c-myc, e.g.GGCTGCTGGAGCGGGGCACAC SEQ ID NO:9AACGTTGAGGGGCAT SEQ ID NO:10d) c-myb, e.g.GTGCCGGGGTCTTCGGGC SEQ ID NO:11GTGCCGGGGTCTTCGGG SEQ ID NO:27e) c-fos, e.g.GGAGAACATCATGGTCGAAG SEQ ID NO:12CCCGAGAACATCATGGTCGAAG SEQ ID NO:13GGGGAAAGCCCGGCAAGGGG SEQ ID NO:14f) p120, e.g.CACCCGCCTTGGCCTCCCAC SEQ ID NO:15g) EGF receptor, e.g.GGGACTCCGGCGAGCGC SEQ ID NO:16GGCAAACTTTCTTTTCCTCC SEQ ID NO:17h) p53 tumor suppressor, e.g.GGGAAGGAGGAGGATGAGG SEQ ID NO:18GGCAGTCATCCAGCTTCGGAG SEQ ID NO:19i) bFGF, e.g.GGCTGCCATGGTCCC SEQ ID NO:31

The pharmaceuticals of the present invention are further suitable, for example, for the treatment of illnesses which are affected by integrins or cell-cell adhesion receptors, for example by VLA-4, VLA-2, ICAM or ELAM.

Sequences according to the invention (base sequences) which are active against targets of this type are, for examplea) VLA-4, e.g.GCAGTAAGCATCCATATC SEQ ID NO:20b) ICAM, e.g.CCCCCACCACTTCCCCTCTC SEQ ID NO:21CTCCCCCACCACTTCCCCTC SEQ ID NO:22GCTGGGAGCCATAGCGAGG SEQ ID NO:23c) ELAM-1, e.g.ACTGCTGCCTCTTGTCTCAGG SEQ ID NO:24CAATCAATGACTTCAAGAGTTC SEQ ID NO:25

The pharmaceuticals of the present invention are further suitable, for example, for the treatment of illnesses which are induced by factors such as TNF alpha.

Sequences according to the invention (base sequences) which are active against targets of this type are, for examplea) TNF-alpha, e.g.TCATGGTGTCCTTTGCAGCC SEQ ID NO:32TCATGGTGTCCTTTGCAG SEQ ID NO:33

The pharmaceuticals can be used, for example, in the form of pharmaceutical preparations which can be administered, for example, topically or orally, e.g. in the form of tablets, coated tablets, hard or soft gelating capsules, solutions, emulsions or suspensions. They can also be administered rectally, e.g. in the form of suppositories, or parenterally, e.g. in the form of injection solutions. For the production of pharmaceutical preparations, these compounds can be processed in therapeutically inert organic and inorganic excipients. Examples of such excipients for tablets, coated tablets and hard gelatin capsules are lactose, maize starch or derivatives thereof, talc and stearic acid or salts thereof. Suitable excipients for the production of solutions are water, polyols, sucrose, invert sugar and glucose. Suitable excipients for injection solutiosn are water, alcohols, polyols, glycerol and vegetble oils. Suitable excipients for suppositories are vegetable and hardened oils, waxes, fats and semiliquid polyols. The pharmaceutical preparations can also contain preservatives, solvents, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorings, salts for changing the osmotic pressure, buffers, coating compositions, antioxidants, and also, if appropriate, other therapeutic active compounds.

A preferred administration is oral administration. A further preferred form of administration is injection. For this, the antisense oligonucleotides are formulated in a liquid solution, preferably in a physiologically acceptable buffer, such as Hank's solution or Ringer's solution. The therapeutically active compounds according to the invention, however, can also be formulated in solid form and dissolved or suspended before use. The preferred dosages for systemic administration are about 0.01 mg/kg to about 50 mg/kg of body weight per day.

List of sequencesACACCCAATTCTGAAAATGG SEQ ID NO:1AGGTCCCTGTTCGGGCGCCA SEQ ID NO:2GTCGACACCCAATTCTGAAAATGGATAA SEQ ID NO:3GCTATGTCGACACCCAATTCTGAAA SEQ ID NO:4GTCGCTGTCTCCGCTTCTTCTTCCTG SEQ ID NO:5GTCTCCGCTTCTTCTTCCTGCCATAGG SEQ ID NO:6GCGGGGCTCCATGGGGGTCG SEQ ID NO:7CAGCTGCAACCCAGC SEQ ID NO:8GGCTGCTGGAGCGGGGCACAC SEQ ID NO:9AACGTTGAGGGGCAT SEQ ID NO:10GTGCCGGGGTCTTCGGGC SEQ ID NO:11GGAGAACATCATGGTCGAAAG SEQ ID NO:12CCCGAGAACATCATGGTCGAAG SEQ ID NO:13GGGGAAAGCCCGGCAAGGGG SEQ ID NO:14CACCCGCCTTGGCCTCCCAC SEQ ID NO:15GGGACTCCGGCGCAGCGC SEQ ID NO:16GGCAAACTTTCTTTTCCTCC SEQ ID NO:17GGGAAGGAGGAGGATGAGG SEQ ID NO:18GGCAGTCATCCAGCTTCGGAG SEQ ID NO:19GCAGTAAGCATCCATATC SEQ ID NO:20CCCCCACCACTTCCCCTCTC SEQ ID NO:21CTCCCCCACCACTTCCCCTC SEQ ID NO:22GCTGGGAGCCATAGCGAGG SEQ ID NO:23ACTGCTGCCTCTTGTCTCAGG SEQ ID NO:24CAATCAATGACTTCAAGAGTTC SEQ ID NO:25GGTCCCTGTTCGGGCGCCA SEQ ID NO:26GTGCCGGGGTCTTCGGG SEQ ID NO:27GGAGGATGCTGAGGAGG SEQ ID NO:28GGAGGATGCTGAGG SEQ ID NO:29CAGGAGGATGCTGAGGAGG SEQ ID NO:30GGCTGCCATGGTCCC SEQ ID NO:31TCATGGTGTCCTTTGCAGCC SEQ ID NO:32TCATGGTGTCCTTTGCAG SEQ ID NO:33

EXAMPLES

1) Di(2-(p-nitrophenyl)ethyl) N-(4-methoxytriphenylmethoxy) ethylaminomethanephosphonate

1a) N-Fluorenylmethoxycarbonyl-2-aminoethanol

8.61 g (0.141 mol) of 2-aminoethanol wer dissolved in 250 ml of dioxane and 150 ml of H₂ O. At 15-20° C., 17.79 g (0.212 mol) of NaHCO₃ were first added, then 50 g (0.148 mol) of fluorenylmethoxycarbonyl-N-succinimide in portions. The mixture was stirred at room temperature for 1 h, then it was evaporated to dryness. The residue was partitioned between dichloromethane (DCM) and H₂ O, the organic phase was dried over Na₂ SO₄ and the solvent was evaporated in vacuo. The residue was stirred with 100 ml of ether, and the product was filtered off with suction and washed well with ether. The yield was 38.77 g (97%).

MS (ES+): 284.2 (M+H)⁺ ; ¹ H-NMR (200 MHz, DMSO, TMS): δ=3.05 (dd, 2H, CH₂ OH); 3.39 (dd, 2H, N═CH₂); 4.25 (m, 3H, Ar--CH--CH₂); 4.61 (t, 1H, OH); 7.14-7.98 (m, 15H, Ar--H, NH).

1b) N-Fluorenylmethoxycarbonyl-2-amino-1-(4-methoxytriphenylmethoxy)ethane

10 g (35.3 mmol) of N-fluorenylmethoxycarbonyl-2-amino-ethanol (from Example 1a), dissolved in 100 ml of absol. N,N-dimethylformamide (DMF), were treated at 0° C. with 5.93 g (45.93 mmol) of diisopropylethylamine (DIPEA) and 10.91 g (35.3 mmol) of 4-methoxytriphenylmethyl chloride and stirred first at 0° C. for 1 h, then at room temperature for 1 h. The reaction mixture was evaporated and partitioned between DCM and a saturated aqueous NaHCO₃ solution. The organic phase was washed with H₂ O and dried over Na₂ SO₄, and the solvent was evaporated in vacuo. To purify the product, it was chromatographed on silica gel (first n-heptane/ethyl acetate (EA)/triethylamine (TEA) 70:29:1; then EA/TEA 99:1). The yield was 14.4 g (73%).

MS (FAB): 562.3 (M+Li)⁺ ; ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.95 (t, 2H, CH₂ O--MMTr); 3.21 (dd, 2H, N--CH₂); 3.75 (s, 3H, OCH₃); 4.25 (m, 3H, Ar--CH--CH₂); 4.61 (t, 1H, OH); 6.80-7.96 (m, 23H, Ar--H, NH).

1c) 2-Amino-1-(4-methoxytriphenylmethoxy)ethane

5.0 g (9 mmol) of N-fluorenylmethoxycarbonyl-2-amino-1-(4-methoxytriphenylmethoxy)ethane (from Example 1b), dissolved in 50 ml of absol. DMF, were treated at room temperature with 6.55 g (90 mmol) of diethylamine and the mixture was stirred for 2 h. To purity it, it was chromatographed on silica gel (first n-heptane/EA/TEA 50:49:1; then EA/methanol/TEA 79:20:1). The yield was 2.96 g (98.7%).

MS (ES+): 340.3 (M+Li)⁺ ; ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.75 (t, 2H, CH₂ O--MMTr); 2.93 (dd, 2H, N--CH₂); 3.75 (s, 3H, OCH₃); 6.83-7.47 (m, 14H, Ar--H).

1d) 2-Methylimino-1-(4-methoxytriphenylmethoxy)ethane (trimer)

2.96 g (8.9 mmol) of 2-amino-1-(4-methoxytriphenylmethoxy)ethane (from Example 1c), dissolved in 10 ml of methanol were treated with ice cooling with 1.08 g (13.22 mmol) of 37% formaldehyde and stirred at room temperature for 4 h, a viscous precipitate being formed. The reaction mixture was evaporated and the residue was chromatographed on silica gel to purify it (n-heptane/EA/TEA 50:49:1). The yield was 1.7 g (55%).

MS (FAB): 1042.8 (M+Li)⁺ ; 1034.8 (M-H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.60 (t, 6H, O--CH₂); 2.99 (t, 6H, N--CH₂); 3.69 (s, 9H, OCH₃); 6.78-7.42 (m, 42H, Ar--H).

1e) Di(2-(4-nitrophenyl)ethyl) phosphite

23.42 g (0.1 mol) of diphenyl phosphite were heated at 100° C. for 14 h under argon together with 33.43 g (0.2 mol) of p-nitrophenylethanol, and to purify it to the mixture was chromatographed on silica gel (n-heptane/EA 50:50; then EA/methanol 80:20). Yield: 55%.

MS (FAB): 403.1 (M+Na)⁺ ; 381.1 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=3.03 (t, 4H, Ar--CH₂); 4.20 (4H, dt, O--CH₂); 6.71 (d, J=140 Hz; 1H; PH); 7.52 (d, 4H, Ar--H); 8.17 (d, 4H, Ar--H).

1f) Di-(2-(p-nitrophenyl)ethyl N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

341 mg (0.329 mmol) of 2-methylimino-1-(4-methoxytriphenylmethoxy)ethane (trimer) (from Example 1d) were added to 500 mg (1.32 mmol) of di(2-(4-nitrophenyl)ethyl) phosphite (from Example 1e), dissolved in 2 ml of absol. Tetrahydrofuran (THF), and the mixture was stirred at 80° C. for 3 h. The solvent was evaporated and the residue was stirred at 100° C. for a further 30 min. To purify it, it was chromatographed on silica gel (first EA/TEA 99:1; then EA/methanol/TEA 90:9:1). Yield: 83%.

MS (FAB): 732.3 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.64-3.06 (m, 10H, Ar--CH₂ +P--CH₂ +CH₂ --OMMTr+N--CH₂); 3.73 (s, 3H, OCH₃); 4.16 (dt, 4H, PO--CH₂); 6.78-8.08 (m, 22H, Ar--H).

2) Di(2-(p-nitrophenyl)ethyl) N-(N⁶ -Anisoyl)cytosin)-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

2a) 0.952 g (8.27 mmol) of N-ethylmorpholine (NEM), 0.834 g (2.76 mmol) of (N⁶ -anisoyl)cytosin-1-yl-acetic acid and 1.153 g (3.03 mmol) of O-(7-aza)benzotriazol-1-yltetramethyluronium hexafluorophosphate (HATU, L. Carpino, J. Am. Chem. Soc. 1993, 115, 4397) was added to 2.00 g (2.76 mmol) of di(2-(p-nitrophenyl)ethyl) N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (from Example 1f), dissolved in 60 ml of absol. DMF, and the mixture was stired at room temperature for 12 h. The same amount of HATU was then added once again and the mixture stirred at room temperature for a further 3 h. To purify it, it was chromatographed on silica gel (DCM/methanol/TEA 95:4:1). The yield was 2.7 g (97%).

MS (ES+): 1012.0 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.94 (t, 4H, P--O--CH₂ --CH₂ --Ar); 3.06 (t, 2H, MMTr--O--CH₂); 3.23-3.63 (m, 4H, P--CH₂ +N--CH₂); 3.76 (s, 3H, OCH₃); 3.83 (s, 3H, OCH₃); 4.10 (dt, 4H, P--O--CH₂); 4.79 (s, broad, 2H, CO--CH₂); 6.80-8.18 (m, 28H, Ar--H, cytosinyl-H); 11.03 (s, broad, 1H, NH).

2b) Mixture as in Example 2a, but using O-(cyano(ethoxycarbonyl)methylamino)-1,1,3,3-tetramethyluronium tetrafluoroborate (TOTU, EP 0460446) instead of HATU. The yield was 57%. Spectroscopic data: see Example 2a.

3) N-(N⁶ -Anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid (2-(p-nitrophenyl)ethyl) monoester (triethylammonium salt)

1 g (0.99 mmol) of di(2-(p-nitrophenyl)ethyl) N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (from Example 2) was dissolved in 20 ml of a 0.1M solution of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in absol. acetonitrile and the mixture was stirred at room temperature for 4 h. The reaction mixture was partitioned between DCM and an aqueous KH₂ PO₄ solution (pH 7), the organic phase was dried over Na₂ SO₄ and the solvent was evaporated in vacuo. To purify the residue, it was chromatographed on silica gel (EA/methanol/TEA 70:29:1). The yield was 540 mg (57%).

MS (FAB): 906.5 (M--H+2Na)⁺ ; 884.6 (M+Na)⁺ ; 862.5 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=3.00 (m, 4H, P--O--CH₂ --CH₂ --Ar+MMTr--O--CH₂); 3.38-3.60 (m, 4H, P--CH₂ +N--CH₂); 3.73 (s, 3H, OCH₃); 3.82 (s, 3H, OCH₃); 4.01 (dt, 2H, P--O--CH₂); 4.79 & 5.03 (in each case s, broad, 2H, CO--CH₂); 6.78-8.20 (m, 24H, Ar--H, cytosinyl-H); 11.00 (s broad, 1H, NH).

4) Di(2-(p-nitrophenyl)ethyl) N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(2-hydroxy)ethylamino-methanephosphonate

1.00 g (0.99 mmol) of di(2-(p-nitrophenyl)ethyl) N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (from Example 2) was dissolved in 80 ml of 80% aqueous acetic acid and the solution was stirred at room temperature for 4 h. The solvent was evaporated and the residue was coevaporated twice with toluene. To purify it, it was chromatographed on silica gel (EA/methanol/TEA 85:14:1). The yield was 522 mg (71%).

MS (FAB): 761.2 (M+Na)⁺ ; 739.3 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.98 (t, 4H, P--O--CH₂ --Ar) 3.38-3.67 (m, 4H, N--CH₂ CH₂ --OH); 3.80-3.89 (m, 2H, P--CH₂); 3.91 (s, 3H, OCH₃); 4.12 (dt, 4H, P--O--CH₂); 4.78 & 4.87 (in each case s, broad, 2H, CO--CH₂); 6.98-8.19 (m, 14H, Ar--H, cytosinyl-H); 11.02 (s, broad, 1H, NH).

5) 5'MMTr-C^(An) -(P(ONPE)-C^(An) -P(ONPE)₂

The synthesis was carried out analogously to Example 7 from N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid (2-(p-nitrophenyl)ethyl monoester (triethylammonium salt) (Example 3) and di(2-(p-nitrophenyl)ethyl) N-(N⁶ -anisoyl) cytosin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 4) To purify it, the compound was chromatrographed on silica gel (EA/methanol/TEA 85/14/1). Yield: 73%.

MS (FAB): 1605 (M+Na)⁺ ; 1583 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.94-3.18 (m, 6H, P--O--CH₂ --CH₂ --Ar) 3.26-3.95 (m, 10H); 3.75 (s, 3H, OCH₃); 3.85 (s, 6H, OCH₃); 3.99-4.36 (m, 8H, P--O--CH₂); 4.75-4.92 (m, broad, 4H, CO--CH₂); 6.83-8.18 (m, 38H, Ar--H, cytosinyl-H); 10.98 & 11.03 (in each case s, broad, 2H, NH).

6) 5'-HO-C^(An) -P(ONPE)-C^(An) -O(ONPE)₂

The synthesis was carried out analogously to Example 4 from "5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (Example 5). To purify it, the compound was chromatographed on silica gel (EA/methanol/TEA 85:14:1). The yield was 74%.

MS (FAB): 1332.4 (M+Na)⁺ ; 1310.3 (M+H)⁺ ;

7) Diethyl N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 1f, but using diethyl phosphite. Yield: 87.5%

MS (FAB): 490.2 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.22 (t, 6H, CH₂ --CH₃); 2.80 (t, 2H, N--CH₂); 2.91 (d, J=12.5 Hz, 2H, P--CH₂); 3.02 (t, 2H, CH₂ --OMMTr); 3.75 (s, 3H, OCH₃); 4.01 (dq, 4H, PO--CH₂); 6.84-7.45 (m, 14H, Ar--H).

8) Diethkyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

570.3 mg (4.22 mmol) of hydroxybenzotriazole (HOBT), 972.1 mg (8.44 mmol) of NEM, 777 mg (4.22 mmol) of thymidin-1-yl-acetic acid and 639 mg (5.06 mmol) of diisopropylcarbodiimide were added to 2.04 g (4.22 mmol) of diethyl N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate Example 7), dissolved in 50 ml of absol. DMF. The mixture was stirred at room temperature for 16 h, the solvent was evaporated, the residue was dissolved in DCM and the solution was extracted with saturated aqueous NaHCO₃ solution, then was saturated with aqueous NaCl solution. The extract was dried over sodium sulfate and the solvent evaported. To purify it, the residue was chromatographed on silica gel (EA/methanol/TEA 98:2:1). The yield was 2.47 g (90%).

MS (FAB): 662.3 (M+Na)⁺ ; 656.3 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.12-1.32 (m, 6H, CH₂ --CH₃); 1.68 & 1.75 (in each case s, 3H, T--CH₃); 3.10-3.40 (m, 2H, CH₂ --OMMTr); 3.53-3.70 (m, 4H, P--CH₂ +N--CH₂); 3.75 (s, 3H, OCH₃); 3.83-4.16 (m, 4H, PO--CH₂); 4.62 & 4.72 (in each case s, 2H, CO--CH₂); 6.83-7.42 (m, 15H, Ar--H, T--H); 11.28 (s, 1H, NH).

9) N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid monoethyl ester (triethylammonium salt)

811 mg (1.25 mmol) of diethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 8) were suspended in 3.75 ml of 1N NaOH. The mixture was stirred at room temperature for 3 h, then at 50° C. for 6 h. The reaction mixture was concentrated in vacuo and the residue was chromatographed on silica gel (EA/methanol/TEA 100:10:10, then 100:40:10). The yield was 897 mg (99.5%).

MS (ES-): 620.4 (M-H)⁻. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.18 (t, 9H, N--CH₂ --CH₃); 1.68 & 1.74 (in each case s, 3H, T--CH₃); 2.96-3.08 (q, 6H, N--CH₂ --CH₃); 3.35 (m, 2H, N--CH₂); 3.43-3.70 (d, J=11 Hz, 2H, P--CH₂); 3.63 (t, 2H, CH₂ --OMMTr); 3.75 (s, 3H, OCH₃); 3.78 (dq, 2H, PO--CH₂); 4.60 & 4.86 (in each case s, 2H, CO--CH₂); 6.82-7.41 (m, 15H, Ar--H, T--H); 11.24 (s, 1H, NH).

10) Diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate

The systhesis was carried out analogously to Example 4 from diethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 8). To purify it, the product was chromatographed on silica gel (EA/methanol 90:10). Yield: 80%.

MS (FAB): 400:1 (M+Na)⁺ ; 378.1 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.17-1.32 (m, 6H, CH₂ --CH₃); 1.78 (s, 3H, T--CH₃); 3.40-3.69 (m, 4H, CH₂ --OH+N--CH₂); 3.89 (d, J=11 Hz, 2H, P--CH₂); 3.92-4.19 (m, 4H, PO--CH₂); 4.70 (s, 2H, CO--CH₂); 4.98 (t, 1H, OH); 7.22 & 7.30 (in each case s, 1H, T--H); 11.25 (s, 1H, NH).

11) Diphenyl N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 1f, but using diethyl phosphite. Yield: 100%.

MS (FAB): 58.2 (M+Li)⁺.

12) N-Thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid monophenyl ester (triethylammonium salt)

The synthesis was carried out analogously to Example 81 from diphenyl N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 11) and thymidin-1-yl-acetic acid. To purify it, the product was chromatographed on silica gel (EA/methanol/TEA/H₂ O 90:10:5:0.5). Yield: 47%.

MS (FAB): 682.3 (M+2Li--H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.16 (t, 9H, N--CH₂ --CH₃); 1.67 & 1.72 (in each case s, 3H, T--CH₃); 2.96-3.70 (m, 12H, N--CH₂ --CH₃ +N--CH₂ +P--CH₂ +CH₂ --OMMTr); 3.75 (s, 3H, OCH₃); 4.58 & 4.88 (in each case s, 2H, CO--CH₂); 6.74-7.46 (m, 20H, Ar--H, T--H); 11.23 (s, 1H, NH).

13) Phenyl 4-nitrophenylethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

385.4 mg (0.5 mmol) of N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid monophenyl ester (triethylammonium salt) (Example 12) and 92 mg (0.55 mmol) of 4-nitrophenylethanol were coevaporated three times with absol. pyridine, then dissolved in 15 ml of absol. pyridine. 403.4 mg (0.15 mmol) of 3-nitro-1-(p-toluenesulfonyl)-1H-1,2,4-triazole (TSNT) were added at 0° C., then the mixture was stirred at 0-5° C. for 16 h, the pyridine was distilled off in vacuo, the residue was taken up in EA and the solution was washed successively with saturated aqueous NaHCO₃ solution, then with NaCl solution. To purify it, the product was charomatographed on silica gel (EA/TEA 100:2). The yield was 162 mg.

MS (FAB): 831.3 (M+2Li--H)⁺ ; (M+Li)⁺.

14) Di(2-(p-nitrophenyl)ethyl) N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 8 from di-(2-(p-nitrophenyl)ethyl) N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 1f) and thymidin 1-yl-acetic acid. Yield: 63%

MS (ES+): 898.4 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.65 & 1.72 (in each case s, 3H, T--CH₃); 2.96 (t, 4H, P--O--CH₂ --CH₂ --Ar); 3.06 (t, 2H, N--CH₂); 3.67 (d, J=11 Hz, 2H, P--CH₂); 3.70 (m, 2H, MMTr--O--CH₂); 3.75 (s, 3H, OCH₃); 3.83 (s, 3H, OCH₃); 4.10 (dt, 4H, P--O--CH₂); 4.59 & 4.62 (in each case s, broad, 2H, CO--CH₂); 6.83-8.18 (m, 23H, Ar--H, T--H); 11.30 (s, broad, 1H, NH).

15) N-Thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt)

15a) From 30 mg of phenyl 4-nitrophenylethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 13)

30 mg of phenyl 4-nitrophenylethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 13) were dissolved in a mixture of 1 ml of TEA, 1 ml of dioxane and 80 mg of p-nitrobenzaldoxime and the solution was stirred at room temperature for 3 h. The solvent was evaporated in vacuo and the residue was coevaporated three times with pyridine and twice with toluene. The residue was chromatographed on silica gel (EA/TEA 100:2, then EA/methanol/TEA 60:40:2). The yield was 23 mg.

MS (FAB): 755.3 (M+2Li--H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.15 (t, 9H, N--CH₂ --CH₃); 1.60 & 1.79 (m, 3H, T--CH₃); 2.80-3.60 (m, 14H, N--CH₂ --CH₃ +N--CH₂ +P--CH₂ +CH₂ --OMMTr+Ar--CH₂); 3.73 (s, 3H, OCH₃); 4.01 (dt, 2H, P--O--CH₂); 4.58-4.92 m, 2H CO--CH₂); 6.82-8.18 (m, 19H, Ar--H, T--H); 11.30 (s, 1H, NH).

15b) From di(2-(p-nitrophenyl)ethyl) N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylamino-methanephosphonate (Example 14)

The synthesis was carried out analogously to Example 3 from di(2-(p-nitrophenyl)ethyl) N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 14), but in pyridine as a solvent. Yield: 82%. Spectrascopic data: see Example 15a.

16) N-Thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid

The synthesis was carried out analogously to Example 15b. N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid is obtained in 18% yield as a by-product.

MS (ES-): 592.2 (M-H)⁻.

17) 5'-MMTr-T-P(O-ethyl)-T-P-(O-ethyl)₂

361 mg (0.5 mmol) of N-thymin-1-yl-acetyl-N-4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid monoethyl ester (triethylammonium salt) (9) and 188.7 mg (0.5 mmol) of diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (10) were coevaporated together twice with absol. pyridine, then dissolved in 10 ml of absol. pyridine. 1.5 mmol of TSNT were added at 5-10° C. and the mixture was stirred at room temperature for 16 h. The pyridine was evaporated in vacuo, the residue was dissolved in EA and the solution was washed successively with saturated aqueous NaHCO₃ solution, then NaCl solution. It was dried over Na₂ SO₄, concentrated and to purify the residue it was chromatographed on silica gel (EA/methanol/TEA 92:8:2). The yield was 223 mg (46%).

MS (FAB): 987.5 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.82-7.43 (m, 16H); CO--CH₂ : 4.59-4.78 (m, 4H); thymine-CH₃ : 1.63-1.80 (m, 6H).

18) 5'-HO-T-P(O-phenyl)-T-P(O-ethyl)₂

The synthesis was carried out analogously to Example 4 from 5'-MMTr-T-P(O-ethyl-T-P(O-ethyl)₂ (Example 17). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 85:15:2, then 100:50:1.5). The yield was 95%.

MS (FAB): 731.2 (M+Na)⁺ 709.1. (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: thymine-H: 7.21-7.36 (m, 2H); CO--CH₂ : 4.60-4.76 (m, 4H); thymine-CH₃ : 1.63-1.79 (m, 6H).

19) 5'-MMTr-T-P(O-phenyl)-T-P(O-ethyl)₂

The synthesis was carried out analogously to Example 17 from diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethyl-aminomethanephosphonate (Example 10) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid monophenyl ester (triethylammonium salt) (Example 12). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 93:7:2). Yield: 58%.

MS (FAB): 1051.4 (M+Na)⁺ ; 1029.5 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.82-7.53 (m, 21H); CO--CH₂ : 4.52-4.82 (m, 4H); thymine-CH₃ : 1.62-1.80 (m, 6H).

20) Di(4-nitrophenylethyl N-thymin-1-yl-acetyl-N-(2-hydroxyethyl)aminomethanephosphonate

The synthesis was carried out analogously to Example 4 from di(2-(p-nitrophenyl)ethyl) N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 14). To purify the product, it was chromatographed on silica gel (EA/methanol 90:10). Yield: 85%.

MS (ES+): 620.3 (M+H)⁺. ¹ H-NMR (500 MHz, DMSO, TMS): δ=1.73 (s, 3H, T--CH₃); 2.97 (t, 4H, P--O--CH₂ --CH₂ --Ar); 3.41 (m, 2H, N--CH₂); 3.59 (m, 2H, CH₂ --OH); 3.83 (d, 2H, J=11 Hz; P--CH₂); 4.08-4.30 (m, 4H, P--O--CH₂); 4.54 & 4.78 (in each case s, broad, 2H, CO--CH₂); 4.99 (t, 1H, OH); 7.14-8.19 (m, 9H, Ar--H, thymidinyl-H); 11.30 (s, broad, 1H, NH).

21) 5'-MMTr-T-P(ONPE)-T-P(O-ethyl)₂

The synthesis was carried out analogously to Example 17 from diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 10) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). Instead of TSNT, 3-nitro-1-(2,4,6-triisopropylphenylsulfonyl)-1H-1,2,4-triazole (TIPSNT) was employed for the coupling. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 95:5:2, then 90:10:2). Yield: >90%.

MS (ES+): 1109.0 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.82-8.18 (m, 20H); CO--CH₂ : 4.51-4.76 (m, 4H); thymine-CH₃ : 1.61-1.78 (m, 6H).

22) 5'-MMTr-T-P(ONPE)-T-P(OEt)₂

The synthesis was carried out analogously to Example 21 from diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 10) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). Instead of TSNT, 3-nitro-1-(2,4,6-triisopropylphenylsulfonyl)-1H-1,2,4-triazole (TIPSNT) was employed for the coupling Yield: >90%.

For spectroscopic data see Example 21.

23) 5'-HO-T-P(ONPE)-T-P(OEt)₂

Synthesis was carried out analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(OEt)₂ " (Example 22). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2, then 80:20:2). The yield was 75%.

MS (ES+): 836.3 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 7.11-8.22 (m, 6H); CO--CH₂ : 4.55-4.77 (m, 4H); thymine-CH₃ :1.71 (s, broad, 6H).

24) 5'-HO-T-P(OH)-T-P(O-ethyl)₂

10 mg (0.012 mmol) of "5'-HO-T-P(ONPE)-T-P(OEt)₂ " (Example 23) were dissolved in 1 ml of a 0.5M solution of DBU in pyridie and stirred first at 4° C. for 24 h, then at room temperature for 24 h. The solvent was evaporated in vacuo, and the residue was digested twice with pentane, then twice with ether, then to purify the product it was chromatographed on silca gel (EA/methanol/TEA 9:1:0.2, then 70:30:2, then 60:40:2). Yield: 10.2 mg.

MS (FAB): 725.3 (M+2Na--H)⁺ ; 703.3 (M+Na)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: thymine-H: 7.15-7.70 (m, 2H); CO--CH₂ : 4.67-4.92 (m, 4H); thymine-CH₃ : 1.67-1.81 (m, 6H).

25) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

The synthesis was carried out analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(OEt)₂ " (Example 22) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15) with addition of 1.5 eq (based on Example 23) of 4-methoxypyridine-N-oxide. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2, then 85:15:2). Yield: 61%.

MS (ES+): 1555.8 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.83-8.20 (m, 25H); CO--CH₂ : 4.52-4.75 (m, 6H); thymine-CH₃ : 1.61-1.78 (m, 9H).

26) 5'-HO-T-P-(ONPE)-T-P(ONPE)-T-P(OEt)₂

The synthesis was carried out analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 25). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2). The yield was 89%.

MS (ES+): 1283.1 (M+H)⁺ ; 1305.0 (M+Na⁺).

27) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

The synthesis was carried out analogously to Example 17 from "5'-HO-T-P-(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 26) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15) with addition of 1.5 eq (based on Example 23) of 4-methoxypyridine-N-oxide. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2, then 80:20:2). Yield: 15%.

MS (ES+): 2007 (M+H)⁺ ; 2029 (M+Na)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.79-8.21 (m, 30H); CO--CH₂ : 4.53-4.87 (m, 8H); thymine-CH₃ : 1.58-1.89 (m, 12H).

28) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

The synthesis was carried out analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 27). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2). The yield was 55%.

MS (FAB): 1735 (M+H)⁺ ; 1757 (M+Na)⁺.

29) 5'-MMTr-T-P(ONPE)-T-P(ONPE)₂

The synthesis was carried out analogously to Example 17 from di(4-nitrophenylethyl) N-thymin-1-yl-acetyl-N-(2hydroxyethyl)aminomethanephosphonate (Example 20) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 100:10:1, then 90:10:1). Yield: 87%.

MS (FAB): 1356.2 (M+2Li--H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar--H & thymine-H: 6.82-8.18 (m, 28H); CO--CH₂ : 4.50-4.71 (m, 4H); thymine-CH₃ : 1.59-1.78 (m, 6H).

30) 5'-HO-T-P(ONPE)-T-P(ONPE)₂

The synthesis was carried out analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)₂ " (Example 29). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 85:15:1, then 80:20:1). The yield was 78%.

MS (ES+): 1072.7 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS) Characteristic signals are: Ar-H & thymine-H: 7.08-8.20 (m, 14H); CO--CH₂ : 4.52-4.80 (m, 4H); thymine-CH₃ : 1.70 (s, broad, 6H).

31) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂

The synthesis was carried out analogously to Example 17 from N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 2-(p-nitropyhenyl)ethyl monoester (triethylammonium salt) (Example 3) and "5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (Example 6). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:19:1). Yield: 66%.

MS (FAB): 2155 (M+H)⁺ ; 2161 (M+Li)⁺ ; 2177 (M+Na)⁺.

32) 5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂

The synthesis was carried out analogously to Example 4 from "5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (Example 31). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 85:15:1, then 80:20:1). The yield was 70%.

MS (FAB): 1882 (M+H)⁺ ; 1904 (M+Na)⁺.

33) Allyl 2-(p-nitrophenyl)ethyl N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 17 from N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 2-(p-nitrophenyl)ethyl monoester (triethylammonium salt) (Example 3) and allyl alcohol. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 95:5:1).

MS (ES+): 902.1 (M+H)⁺ ; 924.1 (M+Na)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.94-3.70 (m, 8H, P--O--CH₂ --Ar+MMTr--O--CH₂ +N--CH₂ +P--CH₂); 3.75 (s, 3H, OCH₃); 3.86 (s, 3H, OCH₃); 4.10-4.60 (m, 4H, P--O--CH₂); 4.79 & 4.84 (in each case s, broad, 2H, CO--CH₂); 5.09-5.39 (m, 2H, H₂ C═CH--); 5.71-6.00 (m, 1H, H₂ C═CH--); 6.83-8.19 (m, 24H, Ar--H, cytosinyl-H); 11.03 (s, broad, 1H, NH).

34) Allyl 2-(p-nitrophenyl)ethyl N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 4 from allyl 2-(p-nitropyenyl)ethyl N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 33). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 94:5:1). The yield was 83%.

MS (ES+): 630.2 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=3.02 (t, 2H, P--O--CH₂ --CH₂ --Ar); 3.37-3.72 (m, 4H, HO--CH₂ CH₂); 3.86 (s, 3H, OCH₃); 3.91 (d, J=11 Hz, 2H, P--CH₂); 4.22 (dt, 2H, P--O--CH₂ --CH₂ --Ar); 4.40 (dd, 2H, O--CH₂ --CH═CH₂); 4.78 & 501 (m, 2H, CO--CH₂); 5.11-5.33 (m, 2H, H₂ C═CH--); 5.71-6.00 (m, 1H, H₂ C═CH--); 6.99-8.21 (m, 14H, Ar--H, cytosinyl-H); 11.03 (s, broad, 1H, NH).

35) Allyl 2-(p-nitrophenyl)ethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

The synthesis was carried out analogously to Example 17 from N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15) and allyl alcohol. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 97:3:2). The yield was 100%.

MS (FAB): 805.3 (M+Na)⁺.

36) Allyl 2-(p-nitrophenyl)ethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate

Synthesis analogously to Example 4 from allyl 2-(p-nitrophenyl)ethyl N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 35). to purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2). The yield was 86%.

MS (ES+): 511.1 (M+H)⁺

37) 5'-MMTr-T-P(ONPE)-T-P(ONPE) (O-allyl)

Synthesis analogously to Example 17 from allyl 2-(p-nitrophenyl)ethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 36) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2). Yield: 90%.

MS (FAB): 1257.3 (M+Na)⁺.

38) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 28) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2). Yield: 57%.

MS (FAB): 2460 (M+H)⁺ ; 2482 (M+Na)⁺.

39) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 38). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2). The yield was 55%.

MS (FAB): 2209 (M+Na)⁺.

40) 5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OEt)₂

4.0 mg (0.00183 mmol) of "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 39) were dissolved in 1.1 ml of a 0.5 molar solution of DBU in pyridine and stirred at room temperature for 24 h. The reaction mixture was evaporated in acuo and the residue was stirred several times with toluene. The solvent was removed using a syringe, the residue was stirred again with pentane, and the solvent was removed again using a syringe. The product was dried in vacuo. The yield was 4 mg of a strongly hygroscopic powder.

MS (ES-): 1589.7 (M-H⁻)⁻ ; 1611.8 (M+Na--2H)⁻.

41) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

a) Synthesis analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P)ONPE)-T-P(OEt)₂ " (Example 39) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2, then 70:30:2).

MS (FAB): 2934 (M+Na)⁺, 2957 (M+2Na--H)⁺, 2978 (M+3Na--2H)⁺.

b) Synthesis analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 28) and "5'-MMTr-T-P(ONPE)-T-P(ONPE) (OH)" (Example 42). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2, then 70:30:2). The target fraction was evaporated in vacuo, then triturated with pentane and ether. MS as above.

42) 5'-MMTr-T-P(ONPE)-T-P(ONPE) (OH)

24.7 mg (0.02 mmol) of "5'-MMTr-T-P(ONPE)-T-P(ONPE) (O-allyl)" (Example 37 ) were dissolved in 2 ml of absol. DCM together with 16.2 mg (0.12 mmol) of diethylammonium hydrogencarbonate. At 15-20° C., a solution of 13.9 mg (0.012 mmol) of tetrakis(triphenylphosphine)palladium (0) and 2.1 mg (0.008 mmol) of triphenylphosphine in 2 ml of absol. DCM was added dropwise during the course of 2 min. The mixture was stirred at room temp. for 30 min. To purify the product, the reaction mixture was chromatographed on silica gel (Ea/methanol/TEA 80:20:1, then 60:40:1). The product fraction was evaporated in vacuo, and the residue was triturated with pentane, then with EA/ether, then again with pentane and dried in vacuo. Yield: 57%.

MS (ES-): 1993.6 (M-H)⁻.

¹ H-NMR (200 MHz, DMSO, TMS): characteristic signals: δ=1.67 & 1.72 (in each case s, 3H, T--CH₃); 4.60 & 4.82 (in each case s, 2H, CO--CH₂); 6.83-8.19 (m, 24H, Ar--H, T--H);

43) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P (ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 41). After reaction had taken place, the reaction mixture was concentrated, and the residue was coevaporated three times with toluene, then stirred, first with EA/ether, then with pentane. The residue was dried in vacuo.

MS (FAB): 2662 (M+Na)⁺.

44) 5'-HO-T-P(ONPE)-T-P(ONPE) (O-allyl)

Synthesis analogously to Example 4 from 5'-MMTr-T-P(ONPE)-T-P(ONPE) (O-allyl) (Example 37). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:1, then 80:20:1). The yield was 87%.

MS (FAB): 963.0 (M+H)⁺ ; 985.1 (M+Na)⁺.

45) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (OH)

a) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (O-allyl)

Synthesis analogously to Example 17 from "5-HO-T-P (ONPE)-T-P(ONPE) (O-allyl)" (Example 44) and N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:1, then 85:15:1). Yield: 55%

b) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (OH)

"5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (O-allyl)" (Example 45a) was reacted with tetrakis(triphenylphosphine)palladium (O) as described in Example 42. To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2, then 70:30:2). The product fraction was evaporated in vacuo, and the residue was triturated with pentane and ether. Yield: 98%.

MS (ES+; LiCl): 1654.1 (M+Li⁺)

46) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 17 from diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethane-phosphonate (Example 10 ) and "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (OH)" (Example 45b). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 90:10:2, then 80:20:2). Working up, purification and characteristics as in Example 27.

47) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 17 from "5'-HO-T-P-(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 26) and "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE (OH)" (Example 45b). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2). The product fraction was evaporated in vacuo, coevaporated with toluene and purified by preparative HPLC (high-pressure liquid chromatography): RP8 LiChrospher 60, water/acetonitrile/:1:1, 0.1% ammonium acetate; 1 ml/min. R_(f) =12.97 min.

48) 5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OEt)₂

a) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P-(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 47). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2, then 60:40:2). The product fraction was evaporated in vacuo, and the residue was stirred, first with pentane, then with ether, and dried in vacuo. Yield: 100%.

MS (FAB): 2662 (M+Na)⁺, 2684 (M+2Na--H)⁺, 2706 (M+3Na--2H)⁺.

b) 5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P-(OEt)₂

"5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 48a) was reacted with DBU and worked up analogously to Example 40.

MS (ES-): 1892 (M-H⁻); 1915 (M+Na-2H)⁻.

49) 5'MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 28) and "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE) (OH)" (Example 45b). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2, then 70:30:2). The product fraction was evaporated in vacuo, coevaporated with toluene and purified by preparative HPLC:RP8 LiChrospher 60, water/acetonitrile: 1:1; 0.1% ammonium acetate; 1 ml/min, R_(f) =15.24 min.

MS (FAB): 3386 (M+Na)⁺, 3409 (M+2Na-H)⁺,

50) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 4 from "5'MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(OEt)₂ " (Example 49). To purify the product, it was evaporated in vacuo and coevaporated three times with toluene, and the residue was stirred, first with pentane, then with ether, and dried in vacuo. Yield: >90%.

MS (FAB): 3114 (M+Na)⁺

51) 5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂

"5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 50) was reacted with DBU and worked up analogously to Example 40.

MS (ES-): 2196 (M-H⁺)⁻ ; 2218 (M+Na-2H)-.

52) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 17 from "5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 48a) and "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)(OH)" (Example 45b). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2, then 60:40:2). The product fraction was evaporated in vacuo, coevaporated with toluene and purified by preparative HPLC: RP8 LiChrospher 60, water/acetonitrile: 1:1; 0.1% ammonium acetate; 1 ml/min. R_(f) =23.95 min.

53) 5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂

a) 5'-HO-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂

Synthesis analogously to Example 4 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(ONPE)-T-P-(ONPE)-T-P(OEt)₂ " (Example 52). To purify the product, it was evaporated in vacuo and coevaporated three times with toluene, and the residue was stirred, first with pentane, then with ether, and dried in vacuo. Yield: <90%.

b) "5'-HO-T-P(OH)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 53a) was reacted with DBU and worked up analogously to Example 40.

MS (ES-): 2802 (M-H⁻)⁻ ; 2825 (M+NA-2H)⁻.

54) Di(2-(p-nitrophenyl)ethyl) 2-(N'-tert-butoxycarbonylamino)ethylaminomethanephosphonate

a) 1-Methylimino-2-(N'-tert-butoxycarbonylamino)ethane (trimer)

2.0 g (12.5 mmol) of 2-amino-1-(N'-tert-butoxycarbonylamino)ethane, dissolved in 8 ml of methanol, were treated with ice cooling with 1.52 ml (18.72 mmol) of 37% formaldehyde and the mixture was stirred at room temp. for 1 h. The residue was taken up in EA, washed twice with saturated NaHCO₃ solution, then with NaCl solution, dried, filtered and evaporated in vacuo. To purify the product, it was chromatographed on silica gel (EA/TEA 100:0.2, then EA/methanol/TEA 90:10:0.2). The yield was 0.8 g.

MS (FAB/LiCl) 523.4 (M+2Li--H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.38 (s, 27H, tBu-H); 2.40 (t, 6H, N-CH₂); 2.99 (t, 6H, N-CH₂); 3.25 (t, 6H, N-CH₂); 6.81 (t, broad, 3H, NH).

b) 2-Di(2-(p-nitrophenyl)ethyl) 2-(N'-tert-butoxycarbonylamino)ethylaminomethanephosphonate

1-Methylimino-2-(N'-tert-butoxycarbonylamino)ethane (trimer) (Example 54a) was reacted with di(2-(4-nitrophenyl)ethyl) phosphite (Example 1e) analogously to Example 1f. To purify the product, it was chromatographed on silica gel (first toluene/EA/TEA 20:80:0.2; then EA/TEA 100:0.2, then EA/methanol/TEA 0.5:5:0.2). Yield: 25%.

MS(ES+LiCl) 553.3 (M+H)⁺, 559.3 M+Li)⁺, ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.37 (s, 9H, tBu-H); 2.83 (d, J=12 Hz, 2H, P-CH₂); 2.55 (t, 4H, Ar-CH₂); 2.90-3.09 (m, 4H, N-CH₂ --CH₂ -N); 4.16 (dt, 4H, PO-CH₂); 7.52 & 8.15 (in each case d, 8H, Ar-H).

55) Di-(2-(p-nitrophenyl)ethyl N-thymin-1yl-acetyl-N-(2-N'-tert-butoxycarbonylamino)ethylaminomethanephosphonate

Synthesis analogously to Example 8 from di(2-(p-nitro-phenyl)ethyl) 2-(N'-tert-butoxycarbonylamino)ethylamino-m-ethanephonate (Example 54b) and thymidin-1-yl-acetic acid.

Yield: 86%

MS (FAB/LiCl): 725.3 (M+Li)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=1.42 (s, 9H, tBu-H); 1.91 (s, 3H, T-CH₃); 2.99-3.58 (m, 8H, P-O-CH₂ -CH₂ -Ar & N-CH₂ --CH₂ -N); 3.75 (d, J=12 Hz, 2H, P-CH₂); 4.06-4.38 (m, 4H, PO-CH₂); 7.37 & 8.15 (in each case d, 8H, Ar-H).

56) Interaction with DNA: UV melting curve

The interaction of the compounds according to the invention with complementary nucleic acids was demonstrated by way of example of the recording of the UV melting curve of "5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P-(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂ " (Example 53b) with (dA)₉. To do this, a 0.3 OD of "5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂ " and (dA)₉ in each case was prepared in 1 ml of a buffer (1M NaCl, 20 mM MgCl₂, 10 mM HEPES, pH 7.5) and the change in extinction at 260 nm was recorded as a function of the temperature (0 to 80° C.). The results can be seen in FIG. 1. A T_(m) value of about 23° C. was determined from the melting curve obtained.

57) Interaction with DNA; gel shift experiment

The interaction of the compounds according to the invention with complementary nucleic acids was demonstrated by way of example by the hybridization of "5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂ " (Example 53b) with (dA)₉ in a gel shift experiment. To do this, "5'-HO-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂ " (Example 53b) and (dA)₉ were in each case applied on their own and mixed in the ratio 1:1, 1:2, 1:5 and 1:10 to a nondenatured polyacrylamide gel (20%, running buffer 1×TBE, 10 mM MgCl₂) and the running behavior determined. The results can be seen in FIG. 2: (dA)₉ runs faster than "5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OEt)₂ " and in the 1:1 mixture both can only be seen weakly, instead a slower band is formed which corresponds to a complex between the two components. In the 2:1 mixture, (dA)₉ can no longer be seen, instead the new band is all the more distinct. The same applies for the 5:1 or 10:1 mixture, in which additionally the distinct excess of "5'-HO-T-P(OH)-T-P(OH)-T-P(OH)-T-P(OH)-T-P-(OH)-T-P(OH)-T-P(OH)-T-P(OEt).sub.2 " can be detected.

58) 5'-MMTr-T-P(ONPE)-T-P(OEthyl)₂ [see also Example 21, alternative syntheses]

a) 8.44 mg (10 μmol) of N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt) (Example 15), 3.77 mg (10 μmol) of diethyl N-thymin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 10) and 64.6 mg (500 μmol) of N-ethyldiisopropylamine (DIPEA) were dissolved in 0.3 ml of absol. DMF. 44.2 mg (100 μmol) of benzotriazolyloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) were added thereto. The mixture was stirred at room temp. for 24 h. About 70% yield according to TLC (EA/methanol/TEA 100:20:2; R_(f) =0.5).

b) Analogously to Example 58a, but using 30 μmol of HATU (O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate) instead of 100 μmol of BOP. About 65% yield according to TLC.

59) 2-(p-Nitrophenyl)ethyl 5'-(3'-levuloyl)thymidine N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate

Synthesis according to Example 17 from N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 4-nitrophenylethyl monoester (triethylammonium salt, Example 15) and 3'-levuloylthymidine. To purify the product, it was chromatographed on silica gel (DCM/methanol/TEA 98:2:0.25). The yield was 46%.

MS (FAB/LiCl): 1071.4 (M+Li)⁺.

60) N-Thymin-1-yl-acetyl-N-(4-methoxy-triphenylmethoxy)ethylaminomethanephosphonic acid 2-(p-nitrophenyl)ethyl 5'-thymidine diester

64 mg (0.06 mmol) of 2-(p-nitrophenyl)ethyl 5'-(3'-levuloyl thymidine N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 59) were dissolved in 0.5 ml of dioxane. 9 mg (0.23 mmol) of NaBH₄ in 0.12 ml of water were added and the mixture was stirred at room temperature for 20 min. The solvent was evaporated in vacuo, the residue was taken up in DCM, and the solution was extracted with water and dried. To purify the product, it was chromatographed on silica gel (DCM/methanol/TEA 92:8:0.5). The yield was 72%.

MS (FAB/LiCl): 973.4 (M+Li)⁺, 979.4 (M+2Li-H)⁺, 985.4 (M+3Li-2H)⁺.

61) N-Thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)-ethylaminomethanephosphonic acid (2-(p-nitrophenyl)ethyl 5'-thymidin-3'-(cyanoethyl-N,N-diisopropyl phosphoramidite)

31 mg (0.032 mmol) of N-thymin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 2-(p-nitrophenyl)ethyl 5'-thymidine diester (Example 60) were coevaporated twice with absol. CH₃ CN and dissolved in 0.4 ml absol. THF. First 12.4 mg (0.096 mmol) of diisopropylethylamine, then 9.8 mg (0.045 mmol) of cyanoethyl chlorodiisopropylphosphoramidite were added thereto. The mixture was stirred for 3 h, filtered and evaporated in vacuo. The yield was 63%.

MS (FAB/LiCl): 1173.3 (M+Li)⁺, 1180.4 (M+2Li-H)⁺, 1186.4 (M+3Li-2H)⁺.

62) Di(2-p-nitrophenyl)ethyl) N-[N9-(O6-diphenylcarbamoyl-N2-acetylguanine]acetyl-N-(4-methoxytriphenyl-methoxy)ethylaminomethanephosphonate

Synthesis analogously to Example 2 from di(2-p-nitrophenyl)ethyl N-(4-methoxytriphenylmethoxy)ethylamino-methanephosphonate (Example 1f) and O6-diphenylcarbamoyl-N2-acetylguanineacetic acid. To purify the product, it was chromatographed on silica gel (EA/TEA 98:2). Yield: 87%

MS (FAB/LiCl): 1154.8 (M+H)⁺, 1160.7 (M+Li)⁺.

63) Di(2-(p-nitrophenyl)ethyl, N-[N9-(N4-anisoyladenine]acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethane-phosponate

Synthesis analogously to Example 2 from di(2-p-nitrophenyl)ethyl, N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 1f) and N4-anisoyladenine-acetic acid. To purify the product, it was chromatographed on silica gel (DCM/methanol/TEA 95:4:1). Yield: 82%; MS (ES+): 1035.7 (M+H)⁺. ¹ H-NMR (200 MHz, DMSO, TMS): δ=2.93 (t, 4H, P-O-CH₂ --CH₂ --Ar); 3.09 (t, 2H, MMTr--O--CH₂); 3.23-3.75 (m, 4H, P--CH₂ +N--CH₂); 3.75 (s, 3H, OCH₃); 3.87 (s, 3H, OCH₃); 4.08 (dt, 4H, P--O--CH₂); 5.28-5.42 (m, 2H, CO--CH₂); 6.81-8.20 (m, 28H, Ar--H, A--H); 11.00 (s broad, 1H, NH).

64) N-[N9-(N4-Anisoyladenine]acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid mono(2-p-nitrophenyl)ethyl ester

Synthesis analogously to Example 3 from di(2-(p-nitrophenyl)ethyl) N-[N9-(N4-anisoyladenine]acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonate (Example 63). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 65:35:2). The yield was 52%.

MS (FAB/LiCl): 874.3 (M+2Li-H)⁺.

65) Di(2-p-nitrophenyl)ethyl), N-thymin-1yl-acetyl-N-(2-methoxy)ethylaminomethanephosphonate

Synthesis analogously to Example 2 from di(2-p-nitrophenyl)ethyl) N-(2-methoxy)ethylaminomethanephosphonate (prepared analogously to Example 1 starting from 2-methoxyethylamine by reaction with formaldehyde and di(2-(4-nitrophenyl)ethyl phosphite) and thymidin-1-yl-acetic acid. To purify the product, it was chromatographed on silica gel (EA/methanol 90:10). Yield: 64%

MS (FAB/LiCl): 640.3 (M+Li)⁺.

66) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OAllyl)

Synthesis analogously to Example 17 from N-(N⁶ -anisoyl)-cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid (2-(p-nitrophenyl)ethyl) monoester (triethylammonium salt) (Example 3) and allyl 2-(p-nitrophenyl)ethyl N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(2-hydroxy)ethylaminomethanephosphonate (Example 34). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 85:14:1). Yield: 36%.

MS (FAB): 1474 (M+H)⁺ ; 1496 (M+Na)⁺.

67) 5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OAllyl)

Synthesis analogously to Example 4 from "5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OAllyl)" (Example 66). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:19:1). The yield was 55%.

MS (FAB): 1201.3 (M+H)⁺, 1223.3 (M+Na)⁺.

68) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE) (O-allyl)

Synthesis analogously to Example 17 from N-(N⁶ -anisoyl)cytosin-1-yl-acetyl-N-(4-methoxytriphenylmethoxy)ethylaminomethanephosphonic acid 2-(p-nitrophenyl)ethyl monester (triethylammonium salt) (Example 3) and 5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OAllyl) (Example 67). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:1). Yield 58%.

MS (FAB): 2046 (M+H)⁺ ; 2068 (M+Na)⁺.

69) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OH)

Synthesis analogously to Example 42 from 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE) (O-allyl) (Example 68). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 60:38:2). Yield: 66%.

MS (FAB): 2027 (M+Na)⁺ ; 2049 (M+2Na--H)⁺.

70) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂

Synthesis analogously to Example 17 from "5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OH)" (Example 69) and "5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (Example 32). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 70:30:2). Yield: 58%.

MS (FAB): 3892 (M+Na)⁺ ; 3914 (M+2Na--H)⁺.

71) 5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂

Synthesis analogously to Example 17 from "5'-MMTr-T-P(ONPE)-T-P-(ONPE)-T-P(ONPE) (OH)" (Example 45) and "5'-HO-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (Example 32). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 60:40:2). The product fraction was evaporated in vacuo and purified by preparative HPLC (high pressure liquid chromatography): RP8 LiChrospher 60, water/acetonitrile: 1:1; 0.1% ammonium acetate; 1 ml/min) R_(f) =16.6 min

MS (FAB): 3534 (M+Na)⁺ ; 3556 (M+2Na--H)⁺.

72) 5'-MMTr-T-P(OH)-T-P(OH)-T-P(OH)-C^(An) -P(OH)-C^(An) -P(OH)-C^(An) -P(OH)₂

Synthesis analogously to Example 40 from "5'-MMTr-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)₂ " (2 mg) (Example 71).

MS (ES-): 2466.4 (M-H).

73) 5'-MMTr-T-P(OH)-T-P(OH)-T-P(OH)-C-P(OH)-C-P(OH)-C-P(OH)₂

About 1 mg of "5'-MMTr-T-P(OH)-T-P-(OH)-T-P(OH)-C^(An) -P(OH)-C^(An) -P(OH)-C^(An) -P(OH)₂ " (Example 72) was treated with 3 ml of 33% aqueous NH₄ OH and stirred at room temperature for 24 h. The reaction mixture was evaporated in vacuo. Yield: about 0.6 mg (19 OD)

MS (ES-): 2064.5 (M-H)⁻.

74) 5'-HO-T-P(OH)-T-P(OH)-C-P(OH)-C-P(OH)-C-P(OH)₂

8 OD of "5'-MMTr-T-P(OH)-T-P(OH)-T-P(OH)-C-P(OH)-C-P(OH)-C-P(OH)₂ " (Example 73) were dissolved in 0.5 ml of water and added to a PolyPak™ (Glen Research, #60-1100-10). The MMTr group was removed following the instructions of the manufacturer (Glen Research User Guide). Yield: about 0.35 mg (11 OD).

MS (ES-: 1792.6 (M-H)⁻.

75) 5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE)-T-P(ONPE)-T-P(ONPE)-T-P(ONPE)₂

Synthesis analogously to Example 17 from "5'-MMTr-C^(An) -P(ONPE)-C^(An) -P(ONPE)-C^(An) -P(ONPE) (OH)" (Example 69) and "5'-HO-T-P-(ONPE)-T-P(ONPE)-T-P(OEt)₂ " (Example 26). To purify the product, it was chromatographed on silica gel (EA/methanol/TEA 80:20:2, then 70:30:2). The product fraction was coevaporated with toluene, evaporated in vacuo and triturated with pentane. Yield: 48%.

MS (FAB): 3744 (M+Na)⁺ ; 3766 (M+2Na-H)⁺.

    __________________________________________________________________________     #             SEQUENCE LISTING                                                 - (1) GENERAL INFORMATION:                                                     -    (iii) NUMBER OF SEQUENCES: 33                                             - (2) INFORMATION FOR SEQ ID NO: 1:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #1:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               ATGG                                                        - (2) INFORMATION FOR SEQ ID NO: 2:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #2:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               GCCA                                                        - (2) INFORMATION FOR SEQ ID NO: 3:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 28 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..28                                                  #3:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #             28   GAAA ATGGATAA                                               - (2) INFORMATION FOR SEQ ID NO: 4:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 25 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..25                                                  #4:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #               25 ATTC TGAAA                                                  - (2) INFORMATION FOR SEQ ID NO: 5:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 26 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..26                                                  #5:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #              26  CTTC TTCCTG                                                 - (2) INFORMATION FOR SEQ ID NO: 6:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 27 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..27                                                  #6:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #             27   CCTG CCATAGG                                                - (2) INFORMATION FOR SEQ ID NO: 7:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #7:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               GTCG                                                        - (2) INFORMATION FOR SEQ ID NO: 8:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 15 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..15                                                  #8:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #    15                                                                        - (2) INFORMATION FOR SEQ ID NO: 9:                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 21 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..21                                                  #9:   (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #21                CACA C                                                      - (2) INFORMATION FOR SEQ ID NO: 10:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 15 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..15                                                  #10:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #    15                                                                        - (2) INFORMATION FOR SEQ ID NO: 11:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 18 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..18                                                  #11:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #  18              GC                                                          - (2) INFORMATION FOR SEQ ID NO: 12:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 21 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..21                                                  #12:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #21                GAAA G                                                      - (2) INFORMATION FOR SEQ ID NO: 13:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 22 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..22                                                  #13:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #                 22CGA AG                                                     - (2) INFORMATION FOR SEQ ID NO: 14:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #14:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               GGGG                                                        - (2) INFORMATION FOR SEQ ID NO: 15:                                           -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #15:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               CCAC                                                        - (2) INFORMATION FOR SEQ ID NO: 16                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 18 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..18                                                  #16:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #  18              GC                                                          - (2) INFORMATION FOR SEQ ID NO: 17                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #17:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               CTCC                                                        - (2) INFORMATION FOR SEQ ID NO: 18                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 19 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..19                                                  #18:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 19               AGG                                                         - (2) INFORMATION FOR SEQ ID NO: 19                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 21 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..21                                                  #19:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #21                CGGA G                                                      - (2) INFORMATION FOR SEQ ID NO: 20                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 18 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..18                                                  #20:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #  18              TC                                                          - (2) INFORMATION FOR SEQ ID NO: 21                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #21:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               TCTC                                                        - (2) INFORMATION FOR SEQ ID NO: 22                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #22:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               CCTC                                                        - (2) INFORMATION FOR SEQ ID NO: 23                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 19 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..19                                                  #23:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 19               AGG                                                         - (2) INFORMATION FOR SEQ ID NO: 24                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 21 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..21                                                  #24:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #21                TCAG G                                                      - (2) INFORMATION FOR SEQ ID NO: 25                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 22 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..22                                                  #25:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #                 22AGT TC                                                     - (2) INFORMATION FOR SEQ ID NO: 26                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 19 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..19                                                  #26:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 19               CCA                                                         - (2) INFORMATION FOR SEQ ID NO: 27                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 17 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..17                                                  #27:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #   17             G                                                           - (2) INFORMATION FOR SEQ ID NO: 28                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 17 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..17                                                  #28:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #   17             G                                                           - (2) INFORMATION FOR SEQ ID NO: 29                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 14 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..14                                                  #29:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #     14                                                                       - (2) INFORMATION FOR SEQ ID NO: 30                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 19 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..19                                                  #30:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 19               AGG                                                         - (2) INFORMATION FOR SEQ ID NO: 31                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 15 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..15                                                  #31:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #    15                                                                        - (2) INFORMATION FOR SEQ ID NO: 32                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 20 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..20                                                  #32:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    # 20               AGCC                                                        - (2) INFORMATION FOR SEQ ID NO: 33                                            -      (i) SEQUENCE CHARACTERISTICS:                                           #pairs    (A) LENGTH: 18 base                                                            (B) TYPE: nucleic acid                                                         (C) STRANDEDNESS: single                                                       (D) TOPOLOGY: linear                                                 -     (ii) MOLECULE TYPE: DNA (genomic)                                        -    (iii) ANTISENSE: yes                                                      -     (ix) FEATURE:                                                                      (A) NAME/KEY: exon                                                             (B) LOCATION: 1..18                                                  #33:  (xi) SEQUENCE DESCRIPTION: SEQ ID NO:                                    #  18              AG                                                          __________________________________________________________________________ 

What is claimed is:
 1. A method for the treatment of viruses comprising the step of administering to a patient in need of such treatment a composition comprising a compound of formula I ##STR37## in which n is a number from zero to 100; A independently of one another is a single bond, a methylene group or a group of formula IIa or Iib; ##STR38## in which M is single bond, --O--, --S-- or --NR¹ --, where R¹ is hydrogen or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio or amino;R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio; p and q independently of one another are zero to 5; and r and s independently of one another are zero to 5; B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl-(C₁ -C₈)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkylthio, an aromatic group or a heterocyclic group, wherein the alkyl, alkyl portion of alkoxy or alkylthio, aromatic or heterocyclic group is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, oxo, --C(O)OR⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₆)-alkoxyalkyl, --S(O)_(m) R⁶, --(C₁ -C₆)-alkyl-S(O)_(m) R⁸, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NR⁹ R¹⁰, --NR⁹ C(═O)NR⁹ R¹⁰, a natural nucleobase, an unnatural nucleobase or a reporter ligand, with the proviso that at least one B moiety is a nucleobase; m is zero, 1 or 2;or, A-B independent of other A and B groups, can be a D- or L-amino acid condensed on via the carboxyl group or a peptide containing amino acids having a length of up to 5 amino acid residues, with the proviso that at least one B moiety is a nucleobase; L independently of one another is N or R¹ N⁺, where R¹ is as defined above; and Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above; D and G each independently represent CR⁵ R⁶ which can be the same or different; R⁵ and R⁶ independently of one another are hydrogen, (C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, wherein the alkyl, alkyl portion of alkoxy or alkylthio, or aryl group is optionally substituted by SR¹ or NR¹ R^(1'), where R¹ is as defined above and R^(1') independently of R¹ has the same meaning as R¹ ; X independently of one another is --O--, --S-- or --NR¹ --, in which R¹ is as defined above; Y independently of one another is ═O or ═S; Z independently of one another is --OR⁸, --NR⁹ R¹⁰ or X'Q", where X' is defined as X above and Q" is defined as Q below; R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, wherein alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and wherein aryl is optionally substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰ ; R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br; or R⁹ and R¹⁰ form a 4 to 7-membered ring together with the N atom in --NR⁹ R¹⁰ ; Q and Q' independently of one another are R⁸, modified or unmodified oligonucleotides or conjugates which a) favorably affect the properties of antisense oligonucleotides, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a label of a DNA probe, or d) during the hybridization of the oligonucleotide analog to the target nucleic acid, attack the target nucleic acid with binding or cross-linking; or Q and Q' alone or together are a single bond in a cyclic molecule; or Q and Q', when neither is hydrogen, can be linked together to form a cyclic molecule;wherein said compound comprises at least 6 nucleotides; together with a physiologically acceptable excipient.
 2. A method for the treatment of cancer or restenosis comprising the step of administering to a patient in need of such treatment an effective amount of a composition comprising a compound of formula I ##STR39## in which n is a number from zero to 100; A independently of one another is a single bond, a methylene group or a group of formula IIa or IIb; ##STR40## in which M is a single bond, --O--, --S-- or --NR¹ --, where R¹ is hydrogen or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio or amino;R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio; p and q independently of one another are zero to 5; and r and s independently of one another are zero to 5; B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkylthio, an aromatic group or a heterocyclic group, wherein the alkyl, alkyl portion of alkoxy or alkylthio, aromatic or heterocyclic group is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, oxo, --C(O)OR⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₆)-alkoxyalkyl, --S(O)_(m) R⁸, --(C₁ -C₆)-alkyl-S(O)_(m) R⁸, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NR⁹ R¹⁰, --NR⁹ C(═O)NR⁹ R¹⁰, a natural nucleobase, an unnatural nucleobase or a reporter ligand, with the proviso that at least one B moiety is a nucleobase; m is zero, 1 or 2;or A-B independent of other A and B groups, can be a D- or L-amino acid condensed on via the carboxy group or a peptide containing amino acids having a length of up to 5 amino acid residues, with the proviso that at least one B moiety is a nucleobase; L independently of one another is N or R¹ N⁺, where R¹ is as defined above; and Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above; D and G each independently represent CR⁵ R⁶ which can be the same or different; R⁵ and R⁶ independently of one another are hydrogen, (C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, wherein the alkyl, alkyl portion of alkoxy or alkylthio, or aryl group is optionally substituted by SR¹ or NR¹ R^(1'), where R¹ is as defined above and R^(1') independently of R¹ has the same meaning as R¹ ; X independently of one another is --O--, --S-- or --NR¹ --, in which R¹ is as defined above; Y independently of one another is ═O or ═S; Z independently of one another is --OR⁸, --NR⁹ R¹⁰ or X'Q", where X' is defined as X above and Q" is defined as Q below; R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, wherein alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and wherein aryl is optionally substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰ ; R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₈ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br; or R⁹ and R¹⁰ form a 4 to 7-membered ring together with the N atom in --NR⁹ R¹⁰ ; Q and Q' independently of one another are R⁸, modified or unmodified oligonucleotides or conjugates which a) favorably affect the properties of antisense oligonucleotides, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a label of a DNA probe, or d) during the hybridization of the oligonucleotide analog to the target nucleic acid, attack the target nucleic acid with binding or cross-linking; or Q and Q' alone or together are a single bond in a cyclic molecule; or Q and Q', when neither is hydrogen, can be linked together to form a cyclic molecule;wherein said compound comprises at least 6 nucleotides; together with a physiologically acceptable excipient.
 3. The method according to claim 1, wherein said virus is HIV, HSV-1, HSV-2, influenza, RSV, hepatitis B, or papilloma virus.
 4. A method for the treatment of medical conditions resulting from integrins or cell-cell adhesion receptors comprising administering to a patient in need of such treatment an effective amount of a composition comprising a compound of formula I ##STR41## in which n is a number from zero to 100; A independently of one another is a single bond, a methylene group or a group of formula IIa or IIb; ##STR42## in which M is a single bond, --O--, --S-- or --NR¹ --, where R¹ is hydrogen or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio or amino;R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio; p and q independently of one another are zero to 5; and r and s independently of one another are zero to 5; B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₈)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkythio, an aromatic group or a heterocyclic group, wherein the alkyl, alkyl portion of alkoxy or alkylthio, aromatic or heterocyclic group is optionally substituted one or more time by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, oxo, --C(O)OR⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₆)-alkoxyalkyl, --S(O)_(m) R⁸, --(C₁ -C₆)-alkyl-S(O)_(m) R⁸, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NR⁹ R¹⁰, --NR⁹ C(═O)NR⁹ R¹⁰, a natural nucleobase, an unnatural nucleobase or a reporter ligand, with the proviso that at least one B moiety is a nucleobase; m is zero, 1 or 2;or, A-B independent of other A and B groups, can be a D- or L-amino acid condensed on via the carboxyl group or a peptide containing amino acids having a length of up to 5 amino acid residues, with the proviso that at least one B moiety is a nucleobase; L independently of one another is N or R¹ N⁺, where R¹ is as defined above; and Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above; D and G each independently represent CR⁵ R⁶ which can be the same or different; R⁵ and R⁶ independently of one another are hydrogen, (C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, wherein the alkyl, alkyl portion of alkoxy or alkylthio, or aryl group is optionally substituted by SR¹ or NR¹ R^(1'), where R¹ is as defined above and R^(1') independently of R¹ has the same meaning as R¹ ; X independently of one another is --O--, --S-- or --NR¹ --, in which R¹ is as defined above; Y independently of one another is ═O or ═S; Z independently of one another is --OR⁸, --NR⁹ R¹⁰ or X'Q", where W' is defined as X above and Q" is defined as Q below; R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, wherein alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and wherein aryl is optionally substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰ ; R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br; or R⁹ and R¹⁰ form a 4 to 7-membered ring together with the N atom in --NR⁹ R¹⁰ ; Q and Q' independently of one another are R⁸, modified or unmodified oligonucleotides or conjugates which a) favorably affect the properties of antisense oligonucleotides, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a label of a DNA probe, or d) during the hybridization of the oligonucleotide analog to the target nucleic acid, attack the target nucleic acid with binding or cross-linking; or Q and Q' alone or together are a single bond in a cyclic molecule; or Q and Q', when neither is hydrogen, can be linked together to form a cyclic molecule;wherein said compound comprises at least 6 nucleotides; together with a physiologically acceptable excipient.
 5. A method for the treatment of medical conditions induced by growth factors comprising the step of administering to a patient in need of such treatment an effective amount of a composition comprising a compound of formula I ##STR43## in which n is a number from zero to 100; A independently of one another is a single bond, a methylene group or a group of formula IIa or IIb; ##STR44## in which M is a single bond, --O--, --S-- or --NR¹ --, where R¹ is hydrogen or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio or amino;R² and R³ independently of one another are hydrogen, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, amino, halogen, or (C₁ -C₆)-alkyl optionally substituted by hydroxyl, (C₁ -C₆)-alkoxy or (C₁ -C₆)-alkylthio; p and q independently of one another are zero to 5; and r and s independently of one another are zero to 5; B independently of one another is hydrogen, hydroxyl, (C₁ -C₂₀)-alkyl, (C₁ -C₂₀)-alkoxy, (C₁ -C₂₀)-alkylthio, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkoxy, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkylthio, an aromatic group or a heterocyclic group, wherein the alkyl, alkyl portion of alkoxy or alkylthio, aromatic or heterocyclic group is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, --NR⁹ R¹⁰, oxo, --C(O)OR⁸, --C(O)NR⁹ R¹⁰, --CN, --F, --Cl, --Br, --NO₂, (C₂ -C₅)-alkoxyalkyl, --S(O)_(m) R⁸, --(C₁ -C₆)-alkyl-S(O)_(m) R⁸, --NHC(═NH)NHR⁸, --C(═NH)NHR⁸, NR⁹ C(═O)R⁸, ═NOR⁸, NR⁹ C(═O)OR¹⁰, --OC(═O)NR⁹ R¹⁰, --NR⁹ C(═O)NR⁹ R¹⁰, a natural nucleobase, an unnatural nucleobase or a reporter ligand, with the proviso that at least one B moiety is a nucleobase; m is zero, 1 or 2;or, A-B independent of other A and B groups, can be a D- or L-amino acid condensed on via the carboxyl group or a peptide containing amino acids having a length of up to 5 amino acid residues, with the proviso that at least one B moiety is a nucleobase; L independently of one another is N or R¹ N⁺, where R¹ is as defined above; and Y' is ═O, ═S, ═CH₂, ═C(CH₃)₂ or ═NR¹, where R¹ is as defined above; D and G each independently represent CR⁵ R⁶ which can be the same or different; R⁵ and R⁶ independently of one another are hydrogen, (C₁ -C₆)-alkyl, (C₆ -C₂₀)-aryl, (C₆ -C₂₀)-aryl-(C₁ -C₆)-alkyl, hydroxyl, (C₁ -C₆)-alkoxy, (C₁ -C₆)-alkylthio, wherein the alkyl, alkyl portion of alkoxy or alkylthio, or aryl group is optionally substituted by SR¹ or NR¹ R^(1'), where R¹ is as defined above and R^(1') independently of R¹ has the same meaning as R¹ ; X independently of one another is --O--, --S-- or --NR¹ --, in which R¹ is as defined above; Y independently of one another is ═O or ═S; Z independently of one another is --OR⁸, --NR⁹ R¹⁰ or X'Q", where X' is defined as X above and Q" is defined as Q below; R⁸ is hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, wherein alkyl is optionally substituted one or more times by hydroxyl, (C₁ -C₄)-alkoxy, F, Cl or Br and wherein aryl is optionally substituted 1-3 times by hydroxyl, (C₁ -C₄)-alkoxy, (C₁ -C₄)-alkyl, F, Cl, Br, NO₂, --NR⁹ R¹⁰, --C(O)OH, --C(O)O--(C₁ -C₆)-alkyl or --C(O)NR⁹ R¹⁰ ; R⁹ and R¹⁰ independently of one another are hydrogen, (C₁ -C₁₈)-alkyl, (C₂ -C₁₈)-alkenyl, (C₃ -C₁₈)-alkynyl, (C₆ -C₁₂)-aryl, (C₆ -C₁₂)-aryl-(C₁ -C₆)-alkyl, where alkyl is optionally substituted one or more time by hydroxy, (C₁ -C₄)-alkoxy, F, Cl or Br; or R⁹ and R¹⁰ form a 4 to 7-membered ring together with the N atom in --NR⁹ R¹⁰ ; Q and Q' independently of one another are R⁸, modified or unmodified oligonucleotides or conjugates which a) favorably affect the properties of antisense oligonucleotides, b) affect the properties of triple helix-forming oligonucleotides, c) serve as a label of a DNA probe, or d) during the hybridization of the oligonucleotide analog to the target nucleic acid, attack the target nucleic acid with binding or cross-linking; or Q and Q' alone or together are a single bond in a cyclic molecule; or Q and Q', when neither is hydrogen, can be linked together to form a cyclic molecule;wherein said compound comprises at least 6 nucleotides; together with a physiologically acceptable excipient.
 6. The method according to claim 5, wherein said growth factor is TNF-α. 